TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777— 510(k) K960196

Name: FDA 510(k) clearance K960196
Creator: U.S. Food and Drug Administration
Published: 1996-02-07

Substantially Equivalent

Tri W-G, Inc.

FDA 510(k) clearance K960196 for TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777, Substantially Equivalent on 1996-02-07. Applicant: Tri W-G, Inc.. Device class: 1.

Clearance details

Applicant: Tri W-G, Inc.
Product code: Code INQ
Device class: Class 1
Regulation: 21 CFR 890.3760
Advisory panel: Physical Medicine
Date received: 1996-01-16
Decision date: 1996-02-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valley City, ND, US

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