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FDA 510(k)

CATHETEO CLAMP

K-Number: K771421 · 1977-10-25

ApplicantQuinton, Inc.
Decision Date1977-10-25
Product CodeFFN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATHETEO CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1977-10-25 under 510(k) number K771421. The device is classified under product code FFN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETEO CLAMP?

CATHETEO CLAMP is a medical device that received FDA 510(k) clearance on 1977-10-25. The listed applicant is Quinton, Inc.. The 510(k) number is K771421.

When did CATHETEO CLAMP receive FDA 510(k) clearance?

CATHETEO CLAMP received FDA 510(k) clearance on 1977-10-25, under 510(k) number K771421.

Who is the listed applicant for CATHETEO CLAMP?

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 CATHETEO CLAMP?

The FDA product code for CATHETEO CLAMP is FFN.

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Other records listing Quinton, Inc. as applicant

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Related Devices (Code: FFN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K932408AMBULATORY INFUSION PUMP SYSTEM AND SOLUTION SETSBaxter Healthcare CorpK892550BEST COLON CLAMPZinnanti Surgical Instruments, Inc.K892542RECTAL SPECULA - CHELSEA-EATON, KELLY, MATHIEUZinnanti Surgical Instruments, Inc.K772405TUBING CLAMPFred Sammons, Inc.

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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