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FDA 510(k)

ONE-HANDED ENDOPOUCH SPECIMEN RETRIEVAL BAG

K-Number: K933104 · 1993-09-13

ApplicantETHICON, Inc.
Decision Date1993-09-13
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ONE-HANDED ENDOPOUCH SPECIMEN RETRIEVAL BAG is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1993-09-13 under 510(k) number K933104. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ONE-HANDED ENDOPOUCH SPECIMEN RETRIEVAL BAG?

ONE-HANDED ENDOPOUCH SPECIMEN RETRIEVAL BAG is a medical device that received FDA 510(k) clearance on 1993-09-13. The listed applicant is ETHICON, Inc.. The 510(k) number is K933104.

When did ONE-HANDED ENDOPOUCH SPECIMEN RETRIEVAL BAG receive FDA 510(k) clearance?

ONE-HANDED ENDOPOUCH SPECIMEN RETRIEVAL BAG received FDA 510(k) clearance on 1993-09-13, under 510(k) number K933104.

Who is the listed applicant for ONE-HANDED ENDOPOUCH SPECIMEN RETRIEVAL BAG?

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

What is the FDA product code for ONE-HANDED ENDOPOUCH SPECIMEN RETRIEVAL BAG?

The FDA product code for ONE-HANDED ENDOPOUCH SPECIMEN RETRIEVAL BAG is GCJ.

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Related Devices (Code: GCJ)

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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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