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FDA 510(k)

SAFE RETURN COT. #9675 & CONNECTOR ADAPT

K-Number: K792044 · 1979-11-16

ApplicantConcept, Inc.
Decision Date1979-11-16
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SAFE RETURN COT. #9675 & CONNECTOR ADAPT is the device name listed in this FDA 510(k) record. The listed applicant is Concept, Inc.. It received FDA 510(k) clearance on 1979-11-16 under 510(k) number K792044. 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 SAFE RETURN COT. #9675 & CONNECTOR ADAPT?

SAFE RETURN COT. #9675 & CONNECTOR ADAPT is a medical device that received FDA 510(k) clearance on 1979-11-16. The listed applicant is Concept, Inc.. The 510(k) number is K792044.

When did SAFE RETURN COT. #9675 & CONNECTOR ADAPT receive FDA 510(k) clearance?

SAFE RETURN COT. #9675 & CONNECTOR ADAPT received FDA 510(k) clearance on 1979-11-16, under 510(k) number K792044.

Who is the listed applicant for SAFE RETURN COT. #9675 & CONNECTOR ADAPT?

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

What is the FDA product code for SAFE RETURN COT. #9675 & CONNECTOR ADAPT?

The FDA product code for SAFE RETURN COT. #9675 & CONNECTOR ADAPT 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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