FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

TRI-TECH URINE SPECIMEN KIT

K Number: K900983 · Decision Sep 17, 1990
Classifications
1
FEI Numbers
294
Registration Numbers
294
Same Product Code
22
Applicant Total
11
Review Days
199

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Basic Information

Device Name
TRI-TECH URINE SPECIMEN KIT
K Number
K900983
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.3250
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Tri-Tech, Inc.
Date Received
March 2, 1990
Decision Date
September 17, 1990
Product Code
FMH
Advisory Committee
Pathology
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FMH Container, Specimen, Sterile

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Other Clearances by Tri-Tech, Inc.

K Number Device Name
K971111 TRI-TECH INC., EVACUATED BLOOD COLLECTION TUBE, GRAY STOPPER
K952246 TRI-TECHIN. CUSTOM BLOOD AND/OR URINE TRANSPORT KIT
K922343 TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT
K922342 TRI-TECH INC. CUSTOM BLOOD ALCOHOL
K912140 STAIRMASTER MODEL 6000 ERGOMETER
K912058 GAUNTLET STAIR CLIMBER
K912056 GRAVITRON UPPER BODY SYSTEM EXERCISER
K912057 4000 PT EXERCISE SYSTEM
K843839 STAT/PB REAGENT
K813075 TRITEC DOC TM
Search all 11 clearances from Tri-Tech, Inc. →