FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

TRI-TECH INC. CUSTOM BLOOD ALCOHOL

K Number: K922342 · Decision Aug 27, 1993
Classifications
1
FEI Numbers
218
Registration Numbers
218
Same Product Code
235
Applicant Total
11
Review Days
465

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Basic Information

Device Name
TRI-TECH INC. CUSTOM BLOOD ALCOHOL
K Number
K922342
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1675
Medical Specialty
Clinical Chemistry
Decision
Unknown
Statement or Summary
Statement
Applicant
Tri-Tech, Inc.
Date Received
May 19, 1992
Decision Date
August 27, 1993
Product Code
JKA
Advisory Committee
Clinical Chemistry
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JKA), ordered by most recent decision date.

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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
K912140 STAIRMASTER MODEL 6000 ERGOMETER
K912058 GAUNTLET STAIR CLIMBER
K912056 GRAVITRON UPPER BODY SYSTEM EXERCISER
K912057 4000 PT EXERCISE SYSTEM
K900983 TRI-TECH URINE SPECIMEN KIT
K843839 STAT/PB REAGENT
K813075 TRITEC DOC TM
Search all 11 clearances from Tri-Tech, Inc. →