MAT TABLE, 8100 SERIES MAT PLATFORM— 510(k) K920585

Name: FDA 510(k) clearance K920585
Creator: U.S. Food and Drug Administration
Published: 1992-04-07

Substantially Equivalent

Tri W-G, Inc.

FDA 510(k) clearance K920585 for MAT TABLE, 8100 SERIES MAT PLATFORM, Substantially Equivalent on 1992-04-07. 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: 1992-02-10
Decision date: 1992-04-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valley City, ND, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code INQ

view all

K960332 — CARDON PHYSICAL THERAPY TABLE MODEL R285981996-02-13
K960334 — CARDON PHYSICAL THERAPY TABLE MODEL R271161996-02-13
K960336 — CARDON PHYSICAL THERAPY TABLE MODEL R276451996-02-13
K960196 — TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 7771996-02-07
K953621 — EVT-33001995-11-14

More clearances from Tri W-G, Inc.

view all

K945163 — ECHOCARDIOGRAPHY1995-02-17
K941720 — MODEL 747 AND 747-30 EXAM/TREATMENT TABLE1994-05-06
K936303 — TREATMENT TABLE MODIFICATION1994-03-18
K933119 — HI-LO TREATMENT TABLES1993-10-12
K932746 — MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE1993-07-21

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