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

OPTICLONE CD3/CD4 MONOCLONAL ANTIBODIES

K Number: K950626 · Decision May 5, 1995
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
376
Applicant Total
37
Review Days
84

Basic Information

Device Name
OPTICLONE CD3/CD4 MONOCLONAL ANTIBODIES
K Number
K950626
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5220
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
IMMUNOTECH CORP.
Date Received
February 10, 1995
Decision Date
May 5, 1995
Product Code
GKZ
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
GKZ Counter, Differential Cell

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K911153 MICROZYME PHENCYCLIDINE ENZYME IMMUNOASSAY TEST KT
K910411 MICROZYME TSH ENZYME IMMUNOASSAY KIT
K905777 MICROZYME THYROID UPTAKE ENZYME IMMUNOASSAY KIT
K903993 MICROZYME(TM) METHAMPHET/AMPHET ENZYME IMMUNO KIT
K904820 MICROZYME T3 ENZYME IMMUNOASSAY KIT
K904635 MICROZYME THC ENZYME IMMUNOASSAY TEST KIT
Search all 37 clearances from IMMUNOTECH CORP. →