PULSE RATE MONITOR— 510(k) K914595

Substantially Equivalent

Fitness Quest, Inc.

FDA 510(k) clearance K914595 for PULSE RATE MONITOR, Substantially Equivalent on 1992-01-31. Applicant: Fitness Quest, Inc.. Device class: 2.

Clearance details

Applicant: Fitness Quest, Inc.
Product code: Code DPZ
Device class: Class 2
Regulation: 21 CFR 870.2710
Advisory panel: Cardiovascular
Date received: 1991-10-16
Decision date: 1992-01-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canton, OH, US

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