MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE— 510(k) K925594

Name: FDA 510(k) clearance K925594
Creator: U.S. Food and Drug Administration
Published: 1993-02-12

Substantially Equivalent

Tri W-G, Inc.

FDA 510(k) clearance K925594 for MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE, Substantially Equivalent on 1993-02-12. 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: 1992-11-05
Decision date: 1993-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valley City, ND, US

Download summary PDF View on FDA.gov ↗

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