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

STREPTOLEX-STAT

K Number: K962296 · Decision Dec 16, 1996
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
104
Applicant Total
73
Review Days
187

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Basic Information

Device Name
STREPTOLEX-STAT
K Number
K962296
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Unipath , Ltd.
Date Received
June 12, 1996
Decision Date
December 16, 1996
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.

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Other Clearances by Unipath , Ltd.

K Number Device Name
K061769 E.P.T. CERTAINTY 1-STEP PREGNANCY TEST
K060128 CLEARBLUE EASY DIGITAL PREGNANCY TEST
K051638 INVERNESS MEDICAL TESTPACK + PLUS STREP A WITH OBC
K050930 E.P.T. CERTAINTY PREGNANCY TEST
K042280 FACT PLUS ONE-STEP PREGNANCY TEST KIT
K041404 CLEARBLUE EASY EASY READ PREGNANCY TEST
K040341 CLEARBLUE EASY EARLIEST RESULTS PREGNANCY TEST
K040329 MODIFICATION TO E.P.T. PREGNANCY TEST
K033658 E.P.T. PREGNANCY TEST
K032939 EPT CERTAINTY PREGNANCY TEST
Search all 73 clearances from Unipath , Ltd. →