SENSOR MOBILE SM 100 VITAPHONE 1001R REMOS— 510(k) K050670

Name: FDA 510(k) clearance K050670
Creator: U.S. Food and Drug Administration
Published: 2005-03-30

Substantially Equivalent

Tms Telemedizinische Systeme GmbH

FDA 510(k) clearance K050670 for SENSOR MOBILE SM 100 VITAPHONE 1001R REMOS, Substantially Equivalent on 2005-03-30. Applicant: Tms Telemedizinische Systeme GmbH. Device class: 2.

Clearance details

Applicant: Tms Telemedizinische Systeme GmbH
Product code: Code DXH
Device class: Class 2
Regulation: 21 CFR 870.2920
Advisory panel: Cardiovascular
Date received: 2005-03-15
Decision date: 2005-03-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chemnitz, DE

Download summary PDF View on FDA.gov ↗

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