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FDA 510(k)

TUBING CLAMP

K-Number: K772405 · 1978-01-26

ApplicantFred Sammons, Inc.
Decision Date1978-01-26
Product CodeFFN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TUBING CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1978-01-26 under 510(k) number K772405. 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 TUBING CLAMP?

TUBING CLAMP is a medical device that received FDA 510(k) clearance on 1978-01-26. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K772405.

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

TUBING CLAMP received FDA 510(k) clearance on 1978-01-26, under 510(k) number K772405.

Who is the listed applicant for TUBING CLAMP?

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

What is the FDA product code for TUBING CLAMP?

The FDA product code for TUBING CLAMP is FFN.

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Other records listing Fred Sammons, 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.K771421CATHETEO CLAMPQuinton, 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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