Medical Device Manufacturer · US , Mchenry , IL

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

29 submissions · 29 cleared · Since 1977

Total

Cleared

Denied

Tri-Med, Inc. has 29 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 29 cleared submissions from 1977 to 2004.

Browse the FDA 510(k) cleared devices submitted by Tri-Med, Inc. Filter by specialty or product code using the sidebar.

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

29 devices

1-12 of 29

General & Plastic Surgery · 14d

Cleared Jan 28, 1988

HUDSON CRANINAL BURRS

K875224 · HBE

Neurology · 37d

Cleared Apr 02, 1985

TRI-MED MODEL 112 MOISTURE TRAP

K850745 · CCK

Anesthesiology · 36d

Cleared Apr 02, 1985

TRI-MED MODEL 126 SAMPLE LINE W/EXTENDED LIFE NAFI

K850746 · CCK

Anesthesiology · 36d

Cleared Apr 02, 1985

TRI-MED MODEL 105 SPECIAL AIRWAY ADAPTOR

K850747 · CCK

Anesthesiology · 36d

Cleared Dec 04, 1984

RESPIRATION & HEART RATE MONITOR 530

K843681 · BZQ

Anesthesiology · 77d

Cleared Nov 13, 1984

TRI-MED 610 CAPNOSTAT GAS ANALYZER

General Hospital · 112d

Cleared Apr 20, 1984

IV-FILTER

K840248 · FPB

General Hospital · 92d

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

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