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

KLEEN TEST BASIN SET

K Number: K890039 · Decision Oct 24, 1989
Classifications
1
FEI Numbers
331
Registration Numbers
331
Same Product Code
83
Applicant Total
17
Review Days
287

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Basic Information

Device Name
KLEEN TEST BASIN SET
K Number
K890039
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Kleen Test Products
Date Received
January 10, 1989
Decision Date
October 24, 1989
Product Code
JOL
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
JOL Catheter And Tip, Suction

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Other Clearances by Kleen Test Products

K Number Device Name
K890539 SURE COUNT LIGHT HANDLE COVER
K890098 KLEEN TEST O.R. KIT
K853622 SURE COUNT 30 COUNT FOAM & MAGNETIC 92-3030
K853454 SURE COUNT 5 & 10 SPONGE COUNTER
K853315 CAUTERY TIP CLEANING PAD
K852258 SURE-COUNT 30 COUNT MAGNETIC NEEDLE COUNTER
K852257 SURE-COUNT 15 COUNT NEEDLE COUNTER
K844199 ELASTIC STYLE IMPERVIOUS ORTHOPEDIC STOCKINET
K821396 OUT-RITE WASTE DISPOSABLE BAG
K821394 SUTURE-SAFE 40 ADHESIVE NEEDLE COUNTER
Search all 17 clearances from Kleen Test Products →