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

STREPTEX ACID EXTRACTION KIT

K Number: K910797 · Decision Mar 29, 1991
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
104
Applicant Total
28
Review Days
31

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Basic Information

Device Name
STREPTEX ACID EXTRACTION KIT
K Number
K910797
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Wellcome Diagnostics
Date Received
February 26, 1991
Decision Date
March 29, 1991
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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K875311 WELLCOZYME HSV WZO2
K861628 WELLCOZYME ROTAVIRUS WZ01
K864206 REVEAL COLOUR STREP A ZL16
K861634 THE WELLCOME ROTAVIRUS LATEX TEST ZL40
K854852 WELLCOGEN BACTERIAL ANTIGEN KIT
K854851 WELLCOGEN N. MENINGITIDIS B/E. COLI K1 ZL24
K851691 WILLCOGEN MENINGITIDIS KIT ZL25
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