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FDA 510(k)

ENDOPATH INTERCEED ABSORBABLE ADHESION BARRIER

K-Number: K920595 · 1993-04-05

ApplicantETHICON, Inc.
Decision Date1993-04-05
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOPATH INTERCEED ABSORBABLE ADHESION BARRIER is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1993-04-05 under 510(k) number K920595. 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 ENDOPATH INTERCEED ABSORBABLE ADHESION BARRIER?

ENDOPATH INTERCEED ABSORBABLE ADHESION BARRIER is a medical device that received FDA 510(k) clearance on 1993-04-05. The listed applicant is ETHICON, Inc.. The 510(k) number is K920595.

When did ENDOPATH INTERCEED ABSORBABLE ADHESION BARRIER receive FDA 510(k) clearance?

ENDOPATH INTERCEED ABSORBABLE ADHESION BARRIER received FDA 510(k) clearance on 1993-04-05, under 510(k) number K920595.

Who is the listed applicant for ENDOPATH INTERCEED ABSORBABLE ADHESION BARRIER?

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 ENDOPATH INTERCEED ABSORBABLE ADHESION BARRIER?

The FDA product code for ENDOPATH INTERCEED ABSORBABLE ADHESION BARRIER is GCJ.

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Related Devices (Code: GCJ)

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Official Source

View on FDA Database →

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

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