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FDA 510(k)

Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis

N.º K: K182272 · 2019-04-15

SolicitanteSterilmed, Inc.
Fecha de decisión2019-04-15
Código de productoNLQ
DecisiónSubstantially Equivalent

Resumen del dispositivo

Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2019-04-15 under 510(k) number K182272. The device is classified under product code NLQ. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis?

Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis is a medical device that received FDA 510(k) clearance on 2019-04-15. The listed applicant is Sterilmed, Inc.. The 510(k) number is K182272.

When did Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis receive FDA 510(k) clearance?

Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis received FDA 510(k) clearance on 2019-04-15, under 510(k) number K182272.

Who is the listed applicant for Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis?

The FDA 510(k) record lists Sterilmed, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis?

The FDA product code for Reprocessed HARMONIC ACE+ 7 Shears with Advanced Hemostasis is NLQ.

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Otros registros que enlistan a Sterilmed, Inc. como solicitante

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

K254149Reprocessed AcuNav CRYSTAL™ Ultrasound Catheter 9F x 90 CM, For Use on Siemens System (R11510825); Reprocessed AcuNav CRYSTAL™ Ultrasound Catheter 9F x 90 CM, For Use on GE System (R11657484); Reprocessed SOUNDSTAR CRYSTAL™ Ultrasound Catheter 9F x 90 CM, For Use on Siemens System (R11510826); Reprocessed SOUNDSTAR CRYSTAL™ Ultrasound Catheter 9F x 90 CM, For Use on GE System (R11657485)K240826Catheter de Electrofisiología DECANAV™ Reciclado; Catheter de Electrofisiología WEBSTER® Duo-Decapolar RecicladoK190478Reprocessed ViewFlex™ Xtra ICE CatheterK190610Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue TechnologyK161700SoundStar eco 8F 3D Diagnostic eco Ultrasound Catheters, SoundStar eco 8F G 3D Diagnostic eco Ultrasound CathetersK161086Reprocessed Harmonic Shears with Adaptive Tissue Technology (36 cm), Reprocessed Harmonic Shears with Adaptive Tissue Technology (23cm)

Ver todos los 10 dispositivos →

Dispositivos relacionados (Código: NLQ)

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

K250898Reprocessed HARMONIC 700 Shears (HAR723/Reprocessed HARMONIC 700, 5mm Diameter Shears with Advanced Hemostasis x 23cm); Reprocessed HARMONIC 700 Shears (HAR736/Reprocessed HARMONIC 700, 5mm Diameter Shears with Advanced Hemostasis x 36cm); Reprocessed HARMONIC 700 Shears (HAR745/Reprocessed HARMONIC 700, 5mm Diameter SHears with Advanced Hemostasis x 45cm)Stryker Sustainability SolutionsK241606Reprocessed HARMONIC 1100 Shears, 5mm Diameter, 20cm Length (HAR1120); Reprocessed HARMONIC 1100 Shears, 5mm Diameter, 36cm Length (HAR1136)Stryker Sustainability SolutionsK233471Reprocessed HARMONIC 1100 Shears, 5mm Diameter, 20cm length (HAR1120); Reprocessed HARMONIC 1100 Shears, 5mm Diameter, 36cm length (HAR1136)Stryker Sustainability SolutionsK202554Reprocessed HARMONIC ACE+ 7, 5 mm Diameter Shears with Advanced HemostasisStryker Sustainability SolutionsK193563Medline ReNewal Reprocessed Harmonic ACE+7 ShearsSurgical Instrument Service and Savings Inc.(Dba Medline RenK190610Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue TechnologySterilmed, Inc.

Fuente oficial

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Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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