RELAXOMAT— 510(k) K925750

Substantially Equivalent

Relaxomat, Inc.

FDA 510(k) clearance K925750 for RELAXOMAT, Substantially Equivalent on 1995-01-31. Applicant: Relaxomat, Inc.. Device class: 2.

Clearance details

Applicant: Relaxomat, Inc.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1992-11-13
Decision date: 1995-01-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tampa, FL, US

Download summary PDF View on FDA.gov ↗

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