DYNATRON 850— 510(k) K941461

Name: FDA 510(k) clearance K941461
Creator: U.S. Food and Drug Administration
Published: 1995-09-01

Substantially Equivalent for Some Indications

Dynatronics Research Corp.

FDA 510(k) clearance K941461 for DYNATRON 850, Substantially Equivalent for Some Indications on 1995-09-01. Applicant: Dynatronics Research Corp.. Device class: 2.

Clearance details

Applicant: Dynatronics Research Corp.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1994-03-24
Decision date: 1995-09-01
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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