ACCU-O-MATIC— 510(k) K841427

Unknown

Myomed, Inc.

FDA 510(k) clearance K841427 for ACCU-O-MATIC, Unknown on 1985-03-05. Applicant: Myomed, Inc.. Device class: 2.

Clearance details

Applicant: Myomed, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1984-04-06
Decision date: 1985-03-05
Decision: Unknown
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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