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FDA 510(k)

SCOVILLE-LEWIS ANEURYSM CLIPS

K-Number: K791764 · 1979-10-01

Decision Date1979-10-01
Product CodeHCH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SCOVILLE-LEWIS ANEURYSM CLIPS 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 1979-10-01 under 510(k) number K791764. The device is classified under product code HCH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCOVILLE-LEWIS ANEURYSM CLIPS?

SCOVILLE-LEWIS ANEURYSM CLIPS is a medical device that received FDA 510(k) clearance on 1979-10-01. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K791764.

When did SCOVILLE-LEWIS ANEURYSM CLIPS receive FDA 510(k) clearance?

SCOVILLE-LEWIS ANEURYSM CLIPS received FDA 510(k) clearance on 1979-10-01, under 510(k) number K791764.

Who is the listed applicant for SCOVILLE-LEWIS ANEURYSM CLIPS?

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

What is the FDA product code for SCOVILLE-LEWIS ANEURYSM CLIPS?

The FDA product code for SCOVILLE-LEWIS ANEURYSM CLIPS is HCH.

Related Clinical Trials

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.

Other records listing Codman & Shurtleff, Inc. as applicant

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.

View all 147 devices →

Related Devices (Code: HCH)

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.

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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