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

MERITEC-STREP GROUP A BETA-HEMOLYTIC

K Number: K831599 · Decision Aug 11, 1983
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
43
Applicant Total
92
Review Days
86

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Basic Information

Device Name
MERITEC-STREP GROUP A BETA-HEMOLYTIC
K Number
K831599
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Meridian Diagnostics, Inc.
Date Received
May 17, 1983
Decision Date
August 11, 1983
Product Code
GTY
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
GTY Antigens, All Groups, Streptococcus Spp.

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K983255 MODIFICATION TO: PREMIER PLATINUM HPSA
K982764 PREMIER CRYPTOSPORIDIUM
K982711 PREMIER GIARDIA
K980076 PREMIER PLATINUM HPSA
K980077 PARA-PAK SPINCON
K971585 IMMUNOCARD STAT! ROTAVIRUS
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