FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

TRITEC DOC TM

K Number: K813075 · Decision Dec 9, 1981
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
459
Applicant Total
11
Review Days
37

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
TRITEC DOC TM
K Number
K813075
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5905
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Tri-Tech, Inc.
Date Received
November 2, 1981
Decision Date
December 9, 1981
Product Code
BZD
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BZD Ventilator, Non-Continuous (Respirator)

Similar 510(k) Clearances

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

View all

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
K900983 TRI-TECH URINE SPECIMEN KIT
K843839 STAT/PB REAGENT
Search all 11 clearances from Tri-Tech, Inc. →