PULSED GALVANIC STIMULATOR, 450-DYNAMAX— 510(k) K801053

Name: FDA 510(k) clearance K801053
Creator: U.S. Food and Drug Administration
Published: 1980-06-04

Substantially Equivalent

U.S. Medical Corp.

FDA 510(k) clearance K801053 for PULSED GALVANIC STIMULATOR, 450-DYNAMAX, Substantially Equivalent on 1980-06-04. Applicant: U.S. Medical Corp.. Device class: 2.

Clearance details

Applicant: U.S. Medical Corp.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1980-05-05
Decision date: 1980-06-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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