FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SURE-STREP A TEST KIT CATALOG NO. MB-1083

K Number: K872346 · Decision Sep 30, 1987
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
104
Applicant Total
39
Review Days
105

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Basic Information

Device Name
SURE-STREP A TEST KIT CATALOG NO. MB-1083
K Number
K872346
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Medix Biotech, Inc.
Date Received
June 17, 1987
Decision Date
September 30, 1987
Product Code
GTZ
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
GTZ Antisera, All Groups, Streptococcus Spp.

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GTZ), ordered by most recent decision date.

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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
K922047 IGE ENZYME IMMUNOASSAY TEST KIT CAT.NO. KIF4064
K921700 TSH ENZYME IMMUNOASSAY TEST KIT CAT. NO. KIF4093
K920712 MEDIX BIOTECH THROXINE ENZYME IMMUNOASSAY TEST KIT
K920345 PROLACTIN ENZYME IMMUNOASSAY TEST KIT (MODIFIED)
Search all 39 clearances from Medix Biotech, Inc. →