SUGITA AVM MICROCLIP— 510(k) K960037

Substantially Equivalent

Mizuho America, Inc.

FDA 510(k) clearance K960037 for SUGITA AVM MICROCLIP, Substantially Equivalent on 1997-02-05. Applicant: Mizuho America, Inc.. Device class: 2.

Clearance details

Applicant: Mizuho America, Inc.
Product code: Code HCH
Device class: Class 2
Regulation: 21 CFR 882.5200
Advisory panel: Neurology
Date received: 1996-01-03
Decision date: 1997-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beverly, MA, 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.