AMS 3000M— 510(k) K936009

Substantially Equivalent

Acutronic Medical Systems AG

FDA 510(k) clearance K936009 for AMS 3000M, Substantially Equivalent on 1995-05-03. Applicant: Acutronic Medical Systems AG. Device class: 2.

Clearance details

Applicant: Acutronic Medical Systems AG
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 1993-12-16
Decision date: 1995-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jona-Rapper Swril, CH

Download summary PDF View on FDA.gov ↗

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