TEC 2100 (MODEL MT-LPLGD)— 510(k) K935760

Substantially Equivalent

Medtec, Inc.

FDA 510(k) clearance K935760 for TEC 2100 (MODEL MT-LPLGD), Substantially Equivalent on 1994-01-25. Applicant: Medtec, Inc.. Device class: 1.

Clearance details

Applicant: Medtec, Inc.
Product code: Code IWE
Device class: Class 1
Regulation: 21 CFR 892.5780
Advisory panel: Radiology
Date received: 1993-11-26
Decision date: 1994-01-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orange City, IA, US

Download summary PDF View on FDA.gov ↗

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