TECA MODEL SP5/T ELECTRO-THER. STIM.— 510(k) K761220

Name: FDA 510(k) clearance K761220
Creator: U.S. Food and Drug Administration
Published: 1976-12-17

Substantially Equivalent

Teca, Inc.

FDA 510(k) clearance K761220 for TECA MODEL SP5/T ELECTRO-THER. STIM., Substantially Equivalent on 1976-12-17. Applicant: Teca, Inc.. Device class: 2.

Clearance details

Applicant: Teca, Inc.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1976-12-07
Decision date: 1976-12-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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