SUNDT-KEES REINFORCING ANEURYSM CLIP
K-Number: K844352 · 1985-01-24
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Device Summary
Frequently Asked Questions
What is the SUNDT-KEES REINFORCING ANEURYSM CLIP?
SUNDT-KEES REINFORCING ANEURYSM CLIP is a medical device that received FDA 510(k) clearance on 1985-01-24. The listed applicant is Kees Surgical Specialty Co., Inc.. The 510(k) number is K844352.
When did SUNDT-KEES REINFORCING ANEURYSM CLIP receive FDA 510(k) clearance?
SUNDT-KEES REINFORCING ANEURYSM CLIP received FDA 510(k) clearance on 1985-01-24, under 510(k) number K844352.
Who is the listed applicant for SUNDT-KEES REINFORCING ANEURYSM CLIP?
The FDA 510(k) record lists Kees Surgical Specialty Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUNDT-KEES REINFORCING ANEURYSM CLIP?
The FDA product code for SUNDT-KEES REINFORCING ANEURYSM CLIP 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.
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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