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FDA 510(k)

REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS

K-Number: K022748 · 2002-10-09

Decision Date2002-10-09
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Services. It received FDA 510(k) clearance on 2002-10-09 under 510(k) number K022748. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS?

REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS is a medical device that received FDA 510(k) clearance on 2002-10-09. The listed applicant is Medical Device Services. The 510(k) number is K022748.

When did REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS receive FDA 510(k) clearance?

REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS received FDA 510(k) clearance on 2002-10-09, under 510(k) number K022748.

Who is the listed applicant for REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS?

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

What is the FDA product code for REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS?

The FDA product code for REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS is HET.

Related Clinical Trials

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.

Other records listing Medical Device Services 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.

Related Devices (Code: HET)

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.

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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