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FDA 510(k)

MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS

K-Number: K030598 · 2004-01-23

ApplicantMedisiss
Decision Date2004-01-23
Product CodeNLQ
DecisionSubstantially Equivalent

Device Summary

MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Medisiss. It received FDA 510(k) clearance on 2004-01-23 under 510(k) number K030598. The device is classified under product code NLQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS?

MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 2004-01-23. The listed applicant is Medisiss. The 510(k) number is K030598.

When did MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS receive FDA 510(k) clearance?

MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS received FDA 510(k) clearance on 2004-01-23, under 510(k) number K030598.

Who is the listed applicant for MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS?

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

What is the FDA product code for MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS?

The FDA product code for MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS is NLQ.

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Other records listing Medisiss as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K113028MEDISISS REPROCESSED ARTHROSCOPIC SHAVERS AND BURSK100543MEDISSISS REPROCESSEDENT ABLATION WANDS (COBLATORS), MODEL#EIC8872-01K081559GENESISK042659MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPSK030919SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES

Related Devices (Code: NLQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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