ClearanceBrief
Company ยท US

Tri-Tech, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1997. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
ISDExerciser, Measuring4
JKATubes, Vials, Systems, Serum Separators, Blood Collection3
BZDVentilator, Non-Continuous (Respirator)1
DOFLead, Atomic Absorption1
FMHContainer, Specimen, Sterile1
JXAKit, Screening, Urine1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 16, 1997K971111TRI-TECH INC., EVACUATED BLOOD COLLECTION TUBE, GRAY STOPPER
Tri-Tech, Inc.
JKA
Jun 20, 1995K952246TRI-TECHIN. CUSTOM BLOOD AND/OR URINE TRANSPORT KIT
Tri-Tech, Inc.
JXA
Feb 17, 1994K922343TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT
Tri-Tech, Inc.
JKA
Aug 27, 1993K922342TRI-TECH INC. CUSTOM BLOOD ALCOHOL
Tri-Tech, Inc.
JKA
Dec 17, 1991K912140STAIRMASTER MODEL 6000 ERGOMETER
Tri-Tech, Inc.
ISD
Oct 24, 1991K912058GAUNTLET STAIR CLIMBER
Tri-Tech, Inc.
ISD
Oct 24, 1991K9120574000 PT EXERCISE SYSTEM
Tri-Tech, Inc.
ISD
Oct 24, 1991K912056GRAVITRON UPPER BODY SYSTEM EXERCISER
Tri-Tech, Inc.
ISD
Sep 17, 1990K900983TRI-TECH URINE SPECIMEN KIT
Tri-Tech, Inc.
FMH
Jan 3, 1985K843839STAT/PB REAGENT
Tri-Tech, Inc.
DOF
Dec 9, 1981K813075TRITEC DOC TM
Tri-Tech, Inc.
BZD

Latest recalls

DateFirm and productCodeLinked 510(k)
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