HORIZON 9000— 510(k) K875167

Substantially Equivalent

Mennen Medical, Inc.

FDA 510(k) clearance K875167 for HORIZON 9000, Substantially Equivalent on 1988-05-31. Applicant: Mennen Medical, Inc.. Device class: 2.

Clearance details

Applicant: Mennen Medical, Inc.
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1987-12-16
Decision date: 1988-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clarence, NY, US

Download summary PDF View on FDA.gov ↗

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More clearances from Mennen Medical, Inc.

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K982697 — MODIFICATION TO ENSEMBLE CENTRAL STATION MONITOR1998-08-12
K974510 — ENVOY PATIENT MONITOR1998-04-14

Data sourced from openFDA. This site is unofficial and independent of the FDA.