DYNATRON 360 RANGE OF MOTION TESTING DEVICE— 510(k) K897178

Name: FDA 510(k) clearance K897178
Creator: U.S. Food and Drug Administration
Published: 1990-04-18

Substantially Equivalent

Dynatronics Corp.

FDA 510(k) clearance K897178 for DYNATRON 360 RANGE OF MOTION TESTING DEVICE, Substantially Equivalent on 1990-04-18. Applicant: Dynatronics Corp.. Device class: 1.

Clearance details

Applicant: Dynatronics Corp.
Product code: Code KQX
Device class: Class 1
Regulation: 21 CFR 888.1500
Advisory panel: Orthopedic
Date received: 1989-12-27
Decision date: 1990-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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