DOUBLE LUMEN E T ADAPTOR— 510(k) K862435

Name: FDA 510(k) clearance K862435
Creator: U.S. Food and Drug Administration
Published: 1986-10-22

Substantially Equivalent

Acutronic Medical Systems AG

FDA 510(k) clearance K862435 for DOUBLE LUMEN E T ADAPTOR, Substantially Equivalent on 1986-10-22. Applicant: Acutronic Medical Systems AG. Device class: 1.

Clearance details

Applicant: Acutronic Medical Systems AG
Product code: Code BZA
Device class: Class 1
Regulation: 21 CFR 868.5810
Advisory panel: Anesthesiology
Date received: 1986-06-26
Decision date: 1986-10-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jona-Rapper Swril, CH

Download summary PDF View on FDA.gov ↗

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