HORIZON 2000 PHYSIOLOGICAL PATIENT MONITOR— 510(k) K850879

Name: FDA 510(k) clearance K850879
Creator: U.S. Food and Drug Administration
Published: 1985-04-25

Substantially Equivalent

Mennen Medical, Inc.

FDA 510(k) clearance K850879 for HORIZON 2000 PHYSIOLOGICAL PATIENT MONITOR, Substantially Equivalent on 1985-04-25. Applicant: Mennen Medical, Inc.. Device class: 2.

Clearance details

Applicant: Mennen Medical, Inc.
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 1985-03-04
Decision date: 1985-04-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clarence, NY, US

Download summary PDF View on FDA.gov ↗

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