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FDA 510(k)

MODIFIED ARTICULATING ENDOSCOPIC CLAMP

K-Number: K925150 · 1993-02-26

ApplicantUnited States Medical Corp.
Decision Date1993-02-26
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODIFIED ARTICULATING ENDOSCOPIC CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is United States Medical Corp.. It received FDA 510(k) clearance on 1993-02-26 under 510(k) number K925150. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED ARTICULATING ENDOSCOPIC CLAMP?

MODIFIED ARTICULATING ENDOSCOPIC CLAMP is a medical device that received FDA 510(k) clearance on 1993-02-26. The listed applicant is United States Medical Corp.. The 510(k) number is K925150.

When did MODIFIED ARTICULATING ENDOSCOPIC CLAMP receive FDA 510(k) clearance?

MODIFIED ARTICULATING ENDOSCOPIC CLAMP received FDA 510(k) clearance on 1993-02-26, under 510(k) number K925150.

Who is the listed applicant for MODIFIED ARTICULATING ENDOSCOPIC CLAMP?

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

What is the FDA product code for MODIFIED ARTICULATING ENDOSCOPIC CLAMP?

The FDA product code for MODIFIED ARTICULATING ENDOSCOPIC CLAMP is GEI.

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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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