DIGITAL ELECTRONIC MYO-GRAPH (MUSCLE ANALYZER)— 510(k) K862128

Name: FDA 510(k) clearance K862128
Creator: U.S. Food and Drug Administration
Published: 1986-07-11

Substantially Equivalent

Health Products, Inc.

FDA 510(k) clearance K862128 for DIGITAL ELECTRONIC MYO-GRAPH (MUSCLE ANALYZER), Substantially Equivalent on 1986-07-11. Applicant: Health Products, Inc.. Device class: 1.

Clearance details

Applicant: Health Products, Inc.
Product code: Code KQX
Device class: Class 1
Regulation: 21 CFR 888.1500
Advisory panel: Orthopedic
Date received: 1986-06-04
Decision date: 1986-07-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hauppauge, NY, US

Download summary PDF View on FDA.gov ↗

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