MICROGAS 7650 TRANSCUTANEOUS MONITOR— 510(k) K003943

Name: FDA 510(k) clearance K003943
Creator: U.S. Food and Drug Administration
Published: 2001-05-04

Substantially Equivalent

Linde Medical Sensors AG

FDA 510(k) clearance K003943 for MICROGAS 7650 TRANSCUTANEOUS MONITOR, Substantially Equivalent on 2001-05-04. Applicant: Linde Medical Sensors AG. Device class: 2.

Clearance details

Applicant: Linde Medical Sensors AG
Product code: Code KLK
Device class: Class 2
Regulation: 21 CFR 868.2500
Advisory panel: Anesthesiology
Date received: 2000-12-21
Decision date: 2001-05-04
Decision: Substantially Equivalent
Clearance type: Special
Location: Basel, CH

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