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

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.

Clearance details

Applicant: Tech Dyne Group
Product code: Code LBB
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 ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.