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

HYDRAGEL IF, 6 IF, 12 IF PENTA KITS/HYDRAGEL IF, DOUBLE IF, 2 IF, & 4 IF KITS

K Number: K960669 · Decision Jul 12, 1996
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
28
Applicant Total
12
Review Days
143

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Basic Information

Device Name
HYDRAGEL IF, 6 IF, 12 IF PENTA KITS/HYDRAGEL IF, DOUBLE IF, 2 IF, & 4 IF KITS
K Number
K960669
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Morax
Date Received
February 20, 1996
Decision Date
July 12, 1996
Product Code
CFF
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
CFF Immunoelectrophoretic, Immunoglobulins, (G, A, M)

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Other Clearances by Morax

K Number Device Name
K033277 HYDRAGEL CSF ISOFOCUSING KITS
K012789 MODIFIED TO LDL/HDL CHOL DIRECT KIT-P.N. 4005, 4103,4123
K992148 HYDRAGEL-MINI ISO-CK KIT, HYDRAGEL ISO-CK KIT, HYDRAGEL 7 IS0-CK KIT, HYDRAGEL ISO-CK 15/30 KIT
K991362 HYDRAGEL HEMOGLOBIN(E), MINI HEMOGLOBIN(E), 7 HEMOGLOBIN(E), 15 HEMOGLOBIN(E), ACID(E) HEMOGLOBIN(E), MINI ACID(E) HEMO)
K990250 HYDRAGEL LDL/HDL CHOL DIRECT KIT-P.N. 4005, HYDRAGEL 7 LDL/HDL CHOL DIRECT KIT-P.N. 4103, HYDRAGEL LDL/HDL CHOL DIRECT 0
K981048 HYDRAGEL 6 CSF KIT
K974854 HYDRAGEL-MINI LIPO KIT-PN 4093, HYDRAGEL LIPO KIT-PN 4007, HYDRAGEL LIPO MAXI KIT-PN 4207
K972591 HYDRAGEL BENCE JONES KIT/MAXI KIT HYDRAGEL BENCE JONES/HYDRAGEL 2/4 BENCE JONES KIT
K972015 HYDRAGEL 7,15,30, CHOL-HDL KIT
K963844 HYDRAGEL 15 HB A1C KIT
Search all 12 clearances from Morax →