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

IGE ENZYME IMMUNOASSAY TEST KIT CAT.NO. KIF4064

K Number: K922047 · Decision Aug 5, 1992
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
113
Applicant Total
39
Review Days
96

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Basic Information

Device Name
IGE ENZYME IMMUNOASSAY TEST KIT CAT.NO. KIF4064
K Number
K922047
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medix Biotech, Inc.
Date Received
May 1, 1992
Decision Date
August 5, 1992
Product Code
DGC
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
DGC Ige, Antigen, Antiserum, Control

Similar 510(k) Clearances

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Other Clearances by Medix Biotech, Inc.

K Number Device Name
K952873 MEDIX BIOTECH STREP A ANTIGEN DETECTION TEST (MODIFICATION)
K952319 CONTRAST & RAPID HCG URINE/SERUM TST
K932482 MEDIX BIOTECH BESTEST STREP A CAT. NO. BSF1010
K932758 MEDIX BIOTECH BESTEST HCG-URINE TEST KIT
K925436 MEDIX BIOTECH TOTAL T3 ENZYME IMMUNOASSAY TEST KIT
K924259 MEDIX BIOTECH BESTEST(TM) HCG-URINE, CAT# B1H0100
K921700 TSH ENZYME IMMUNOASSAY TEST KIT CAT. NO. KIF4093
K920712 MEDIX BIOTECH THROXINE ENZYME IMMUNOASSAY TEST KIT
K920345 PROLACTIN ENZYME IMMUNOASSAY TEST KIT (MODIFIED)
K920299 MEDIX BIOTECH HGHENZYME IMMUNOASSAY TEST KIT
Search all 39 clearances from Medix Biotech, Inc. →