DYNATRON 1120 EPS (ELECTRICAL POINT STIMULATOR)— 510(k) K864370

Name: FDA 510(k) clearance K864370
Creator: U.S. Food and Drug Administration
Published: 1987-04-10

Substantially Equivalent for Some Indications

Dynatronics Laser Corp.

FDA 510(k) clearance K864370 for DYNATRON 1120 EPS (ELECTRICAL POINT STIMULATOR), Substantially Equivalent for Some Indications on 1987-04-10. Applicant: Dynatronics Laser Corp.. Device class: 2.

Clearance details

Applicant: Dynatronics Laser Corp.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1986-11-05
Decision date: 1987-04-10
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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