DYNATRON 2000— 510(k) K880912

Substantially Equivalent

Dynatronics Corp.

FDA 510(k) clearance K880912 for DYNATRON 2000, Substantially Equivalent on 1988-03-15. Applicant: Dynatronics Corp.. Device class: 1.

Clearance details

Applicant: Dynatronics Corp.
Product code: Code IKE
Device class: Class 1
Regulation: 21 CFR 890.1615
Advisory panel: Physical Medicine
Date received: 1988-03-03
Decision date: 1988-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.