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FDA 510(k)

TUBE OCCLUDING FORCEPS

K-Number: K771424 · 1977-08-26

ApplicantQuinton, Inc.
Decision Date1977-08-26
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TUBE OCCLUDING FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1977-08-26 under 510(k) number K771424. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBE OCCLUDING FORCEPS?

TUBE OCCLUDING FORCEPS is a medical device that received FDA 510(k) clearance on 1977-08-26. The listed applicant is Quinton, Inc.. The 510(k) number is K771424.

When did TUBE OCCLUDING FORCEPS receive FDA 510(k) clearance?

TUBE OCCLUDING FORCEPS received FDA 510(k) clearance on 1977-08-26, under 510(k) number K771424.

Who is the listed applicant for TUBE OCCLUDING FORCEPS?

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

What is the FDA product code for TUBE OCCLUDING FORCEPS?

The FDA product code for TUBE OCCLUDING FORCEPS is KOC.

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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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