MICROGAS 7650 TRANSCUTANEOUS MONITOR— 510(k) K991644

Name: FDA 510(k) clearance K991644
Creator: U.S. Food and Drug Administration
Published: 1999-05-21

Substantially Equivalent

Linde Medical Sensors AG

FDA 510(k) clearance K991644 for MICROGAS 7650 TRANSCUTANEOUS MONITOR, Substantially Equivalent on 1999-05-21. 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: 1999-05-13
Decision date: 1999-05-21
Decision: Substantially Equivalent
Clearance type: Special
Location: Basel, CH

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