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FDA 510(k)

SUGITA ANEURYSM CLIPS, APPLIERS & CASE

K-Number: K791978 · 1979-09-28

ApplicantCodman & Shurtleff, Inc.
Decision Date1979-09-28
Product Code
DecisionUnknown

Device Summary

SUGITA ANEURYSM CLIPS, APPLIERS & CASE is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1979-09-28 under 510(k) number K791978. FDA Decision: Unknown.

Frequently Asked Questions

What is the SUGITA ANEURYSM CLIPS, APPLIERS & CASE?

SUGITA ANEURYSM CLIPS, APPLIERS & CASE is a medical device that received FDA 510(k) clearance on 1979-09-28. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K791978.

When did SUGITA ANEURYSM CLIPS, APPLIERS & CASE receive FDA 510(k) clearance?

SUGITA ANEURYSM CLIPS, APPLIERS & CASE received FDA 510(k) clearance on 1979-09-28, under 510(k) number K791978.

Who is the listed applicant for SUGITA ANEURYSM CLIPS, APPLIERS & CASE?

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

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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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