MODEL RF-TENS-4 TRANSCUTANEOUS ELEC. NERVE STIMULA— 510(k) K853885

Name: FDA 510(k) clearance K853885
Creator: U.S. Food and Drug Administration
Published: 1986-01-30

Substantially Equivalent

Uniking Intl. Corp.

FDA 510(k) clearance K853885 for MODEL RF-TENS-4 TRANSCUTANEOUS ELEC. NERVE STIMULA, Substantially Equivalent on 1986-01-30. Applicant: Uniking Intl. Corp.. Device class: 2.

Clearance details

Applicant: Uniking Intl. Corp.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1985-09-19
Decision date: 1986-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Torrance, CA, US

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