FDA 510(k)

Sonopet iQ Ultrasonic Aspirator System (5500-050-000)

Número K: K243930 · 2025-03-24

Data da decisão2025-03-24

Código do produtoLFL

DecisãoSubstantially Equivalent

Resumo do dispositivo

Sonopet iQ Ultrasonic Aspirator System (5500-050-000) is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 2025-03-24 under 510(k) number K243930. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Sonopet iQ Ultrasonic Aspirator System (5500-050-000)?

Sonopet iQ Ultrasonic Aspirator System (5500-050-000) is a medical device that received FDA 510(k) clearance on 2025-03-24. The listed applicant is Stryker Instruments. The 510(k) number is K243930.

When did Sonopet iQ Ultrasonic Aspirator System (5500-050-000) receive FDA 510(k) clearance?

Sonopet iQ Ultrasonic Aspirator System (5500-050-000) received FDA 510(k) clearance on 2025-03-24, under 510(k) number K243930.

Who is the listed applicant for Sonopet iQ Ultrasonic Aspirator System (5500-050-000)?

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

What is the FDA product code for Sonopet iQ Ultrasonic Aspirator System (5500-050-000)?

The FDA product code for Sonopet iQ Ultrasonic Aspirator System (5500-050-000) is LFL.

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Fonte oficial

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