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

CLEAR POROUS PLASTIC-HYPOALLERGENIC

K Number: K840948 · Decision Aug 14, 1984
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
1
Applicant Total
11
Review Days
39

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Basic Information

Device Name
CLEAR POROUS PLASTIC-HYPOALLERGENIC
K Number
K840948
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5200
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Gainor Medical
Date Received
July 6, 1984
Decision Date
August 14, 1984
Product Code
GKX
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
GKX Instrument, Automated Platelet Counting

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Other Clearances by Gainor Medical

K Number Device Name
K850100 BLOOD LANCET
K850150 ULSTER SCIENTIFIC, INC. AUTOLET LANCETS/GAINOR MED
K844306 GAINOR MEDICAL SYRINGE
K844305 GAINOR MEDICAL FLOWMAX NEEDLES
K840951 FIRST AID BANDAGE
K840950 ZINC OXIDE TAPE
K840945 SKIN CLOSURE
K840947 CLOTH-HYPOALLERGENIC
K840949 CLEAR PLASTIC-HYPOALLERGENIC
K840946 MICROPOROUS HYPOALLERGENIC
Search all 11 clearances from Gainor Medical →