T.E.N.S. DEVICE MODEL SPL 2000S— 510(k) K872399

Name: FDA 510(k) clearance K872399
Creator: U.S. Food and Drug Administration
Published: 1987-07-27

Substantially Equivalent

Spartan Laboratories, Inc.

FDA 510(k) clearance K872399 for T.E.N.S. DEVICE MODEL SPL 2000S, Substantially Equivalent on 1987-07-27. Applicant: Spartan Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Spartan Laboratories, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1987-06-22
Decision date: 1987-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Las Vegas, NV, US

Download summary PDF View on FDA.gov ↗

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