SUNDT-KEES REINFORCING ANEURYSM CLIP— 510(k) K844352

Name: FDA 510(k) clearance K844352
Creator: U.S. Food and Drug Administration
Published: 1985-01-24

Substantially Equivalent

Kees Surgical Specialty Co., Inc.

FDA 510(k) clearance K844352 for SUNDT-KEES REINFORCING ANEURYSM CLIP, Substantially Equivalent on 1985-01-24. Applicant: Kees Surgical Specialty Co., Inc.. Device class: 2.

Clearance details

Applicant: Kees Surgical Specialty Co., Inc.
Product code: Code HCH
Device class: Class 2
Regulation: 21 CFR 882.5200
Advisory panel: Neurology
Date received: 1984-11-09
Decision date: 1985-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wilder, KY, US

Download summary PDF View on FDA.gov ↗

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K081640 — GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS2009-05-06

Data sourced from openFDA. This site is unofficial and independent of the FDA.