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

KLEEN TEST O.R. KIT

K Number: K890098 · Decision Jan 24, 1989
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
109
Applicant Total
17
Review Days
14

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Basic Information

Device Name
KLEEN TEST O.R. KIT
K Number
K890098
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Kleen Test Products
Date Received
January 10, 1989
Decision Date
January 24, 1989
Product Code
LRO
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
LRO General Surgery Tray

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Other Clearances by Kleen Test Products

K Number Device Name
K890039 KLEEN TEST BASIN SET
K890539 SURE COUNT LIGHT HANDLE COVER
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 →