SYSTEM ATHENA-PRODUCT ENHANCEMENTS, ANESTHESIA— 510(k) K912145

Name: FDA 510(k) clearance K912145
Creator: U.S. Food and Drug Administration
Published: 1992-05-05

Substantially Equivalent

S & W Medico Teknik

FDA 510(k) clearance K912145 for SYSTEM ATHENA-PRODUCT ENHANCEMENTS, ANESTHESIA, Substantially Equivalent on 1992-05-05. Applicant: S & W Medico Teknik. Device class: 2.

Clearance details

Applicant: S & W Medico Teknik
Product code: Code CCE
Device class: Class 2
Regulation: 21 CFR 868.1200
Advisory panel: Anesthesiology
Date received: 1991-04-09
Decision date: 1992-05-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denmark, DK

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