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

STAPH KIT

K Number: K853488 · Decision Aug 28, 1985
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
284
Applicant Total
9
Review Days
8

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Basic Information

Device Name
STAPH KIT
K Number
K853488
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2360
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Culture Kits, Inc.
Date Received
August 20, 1985
Decision Date
August 28, 1985
Product Code
JSI
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
JSI Culture Media, Selective And Differential

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Other Clearances by Culture Kits, Inc.

K Number Device Name
K911846 URI-THREE(TM), MODIFICATION
K854672 CANDI-KIT TM
K851225 URINE DUO
K852582 GONI-KIT
K852480 DERM-KIT
K851518 MUELLER HINTON SENSITIVITY PLATE
K850765 STREP-KIT
K850998 URI-KIT