DYNO-MAX II - COMPUTERIZED MUSCLE ANALYZER— 510(k) K872199

Name: FDA 510(k) clearance K872199
Creator: U.S. Food and Drug Administration
Published: 1987-08-21

Substantially Equivalent

Dyno-Max Co.

FDA 510(k) clearance K872199 for DYNO-MAX II - COMPUTERIZED MUSCLE ANALYZER, Substantially Equivalent on 1987-08-21. Applicant: Dyno-Max Co.. Device class: 2.

Clearance details

Applicant: Dyno-Max Co.
Product code: Code IKK
Device class: Class 2
Regulation: 21 CFR 890.1925
Advisory panel: Physical Medicine
Date received: 1987-06-08
Decision date: 1987-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Richmond, CA, US

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