TECH DYNE - HP-2000, SKREEN TEST, RMS-200— 510(k) K920183

Name: FDA 510(k) clearance K920183
Creator: U.S. Food and Drug Administration
Published: 1992-06-15

Substantially Equivalent

Tech Dyne Group

FDA 510(k) clearance K920183 for TECH DYNE - HP-2000, SKREEN TEST, RMS-200, Substantially Equivalent on 1992-06-15. Applicant: Tech Dyne Group. Device class: 2.

Clearance details

Applicant: Tech Dyne Group
Product code: Code LBB
Device class: Class 2
Regulation: 21 CFR 888.1240
Advisory panel: Orthopedic
Date received: 1992-01-15
Decision date: 1992-06-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sherman, TX, US

Download summary PDF View on FDA.gov ↗

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