Medical Device Manufacturer · US , Mchenry , IL

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

11 submissions · 9 cleared · Since 1981

11

Total

9

Cleared

0

Denied

Tri-Tech, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1981 to 1997.

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

Tri-Tech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

11 devices

1-11 of 11

Cleared Jun 16, 1997

TRI-TECH INC., EVACUATED BLOOD COLLECTION TUBE, GRAY STOPPER

Chemistry · 82d

Cleared Jun 20, 1995

TRI-TECHIN. CUSTOM BLOOD AND/OR URINE TRANSPORT KIT

Chemistry · 39d

Cleared Feb 17, 1994

TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT

Toxicology · 639d

Cleared Aug 27, 1993

TRI-TECH INC. CUSTOM BLOOD ALCOHOL

Toxicology · 465d

Cleared Dec 17, 1991

STAIRMASTER MODEL 6000 ERGOMETER

Physical Medicine · 217d

Cleared Oct 24, 1991

GRAVITRON UPPER BODY SYSTEM EXERCISER

Physical Medicine · 168d

Cleared Oct 24, 1991

4000 PT EXERCISE SYSTEM

Physical Medicine · 168d

Cleared Oct 24, 1991

GAUNTLET STAIR CLIMBER

Physical Medicine · 168d

Cleared Sep 17, 1990

TRI-TECH URINE SPECIMEN KIT

Chemistry · 199d

Cleared Jan 03, 1985

STAT/PB REAGENT

Chemistry · 94d

Cleared Dec 09, 1981

Anesthesiology · 37d