MICROCO— 510(k) K950197

Substantially Equivalent

Micro Direct, Inc.

FDA 510(k) clearance K950197 for MICROCO, Substantially Equivalent on 1996-10-17. Applicant: Micro Direct, Inc.. Device class: 2.

Clearance details

Applicant: Micro Direct, Inc.
Product code: Code CCJ
Device class: Class 2
Regulation: 21 CFR 868.1430
Advisory panel: Anesthesiology
Date received: 1995-01-18
Decision date: 1996-10-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Auburn, ME, 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.