MODEL 219 TELEMETRY SYSTEM— 510(k) K895895

Name: FDA 510(k) clearance K895895
Creator: U.S. Food and Drug Administration
Published: 1990-02-22

Substantially Equivalent

Mennen Medical, Inc.

FDA 510(k) clearance K895895 for MODEL 219 TELEMETRY SYSTEM, Substantially Equivalent on 1990-02-22. Applicant: Mennen Medical, Inc.. Device class: 2.

Clearance details

Applicant: Mennen Medical, Inc.
Product code: Code GYE
Device class: Class 2
Regulation: 21 CFR 882.1855
Advisory panel: Neurology
Date received: 1989-10-06
Decision date: 1990-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clarence, NY, US

Download summary PDF View on FDA.gov ↗

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