DS-200 AND DS-400 T.E.N.S.— 510(k) K881832

Name: FDA 510(k) clearance K881832
Creator: U.S. Food and Drug Administration
Published: 1988-07-01

Substantially Equivalent

Delta Marketing, Inc.

FDA 510(k) clearance K881832 for DS-200 AND DS-400 T.E.N.S., Substantially Equivalent on 1988-07-01. Applicant: Delta Marketing, Inc.. Device class: 2.

Clearance details

Applicant: Delta Marketing, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1988-04-29
Decision date: 1988-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Muskogee, OK, US

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