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FDA 510(k)

REPROCESSED DISPOSABLE TROCARS

K-Number: K022743 · 2002-10-09

Decision Date2002-10-09
Product CodeKAB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

REPROCESSED DISPOSABLE TROCARS 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 K022743. The device is classified under product code KAB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED DISPOSABLE TROCARS?

REPROCESSED DISPOSABLE TROCARS 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 K022743.

When did REPROCESSED DISPOSABLE TROCARS receive FDA 510(k) clearance?

REPROCESSED DISPOSABLE TROCARS received FDA 510(k) clearance on 2002-10-09, under 510(k) number K022743.

Who is the listed applicant for REPROCESSED DISPOSABLE TROCARS?

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 REPROCESSED DISPOSABLE TROCARS?

The FDA product code for REPROCESSED DISPOSABLE TROCARS is KAB.

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.

Official Source

View on FDA Database →

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