SCOVILLE-LEWIS ANEURYSM CLIPS
K-Number: K791764 · 1979-10-01
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Device Summary
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.
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
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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