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FDA 510(k)

ENDOPATH EP DISPOSABLE TROCAR

K-Number: K922608 · 1993-10-12

ApplicantETHICON, Inc.
Decision Date1993-10-12
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOPATH EP DISPOSABLE TROCAR is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1993-10-12 under 510(k) number K922608. 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 EP DISPOSABLE TROCAR?

ENDOPATH EP DISPOSABLE TROCAR is a medical device that received FDA 510(k) clearance on 1993-10-12. The listed applicant is ETHICON, Inc.. The 510(k) number is K922608.

When did ENDOPATH EP DISPOSABLE TROCAR receive FDA 510(k) clearance?

ENDOPATH EP DISPOSABLE TROCAR received FDA 510(k) clearance on 1993-10-12, under 510(k) number K922608.

Who is the listed applicant for ENDOPATH EP DISPOSABLE TROCAR?

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 EP DISPOSABLE TROCAR?

The FDA product code for ENDOPATH EP DISPOSABLE TROCAR 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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