Medical Device Manufacturer · US , Mchenry , IL

Tri W-G, Inc. - FDA 510(k) Cleared Devices

35 submissions · 35 cleared · Since 1979

Total

Cleared

Denied

Tri W-G, Inc. has 35 FDA 510(k) cleared physical medicine devices. Based in Mchenry, US.

Historical record: 35 cleared submissions from 1979 to 1996.

Browse the complete list of FDA 510(k) cleared physical medicine devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Tri W-G, Inc.

35 devices

1-12 of 35

Cleared Feb 07, 1996

TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777

K960196 · INQ

Physical Medicine · 22d

Cleared Feb 17, 1995

ECHOCARDIOGRAPHY

K945163 · LGX

General Hospital · 119d

Cleared May 06, 1994

MODEL 747 AND 747-30 EXAM/TREATMENT TABLE

K941720 · INQ

Physical Medicine · 29d

Cleared Mar 18, 1994

TREATMENT TABLE MODIFICATION

K936303 · INQ

Physical Medicine · 119d

Cleared Oct 12, 1993

HI-LO TREATMENT TABLES

K933119 · INQ

Physical Medicine · 109d

Cleared Jul 21, 1993

MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE

K932746 · INQ

Physical Medicine · 43d

Cleared Mar 22, 1993

MODELS 642 & 643 TILT EXAM/TREATMENT TABLE

K930802 · INQ

Physical Medicine · 34d

Cleared Feb 12, 1993

MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE

K925594 · INQ

Physical Medicine · 99d

Cleared Jul 21, 1992

MODEL 600 MEDICAL TREATMENT TABLE

K923325 · INQ

Physical Medicine · 14d

Cleared Jul 13, 1992

745-M (MAGNUM)

K922980 · JFB

Physical Medicine · 21d

Cleared Apr 07, 1992

MAT TABLE, 8100 SERIES MAT PLATFORM

K920585 · INQ

Physical Medicine · 57d

Tri W-G, Inc. - FDA 510(k) Cleared Devices

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