SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM— 510(k) K960372

Name: FDA 510(k) clearance K960372
Creator: U.S. Food and Drug Administration
Published: 1996-04-26

Substantially Equivalent

Scanlan Intl., Inc.

FDA 510(k) clearance K960372 for SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM, Substantially Equivalent on 1996-04-26. Applicant: Scanlan Intl., Inc.. Device class: 2.

Clearance details

Applicant: Scanlan Intl., Inc.
Product code: Code HCH
Device class: Class 2
Regulation: 21 CFR 882.5200
Advisory panel: Neurology
Date received: 1996-01-26
Decision date: 1996-04-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Saint Paul, MN, US

Download summary PDF View on FDA.gov ↗

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