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

M. CAT BUTYRATE DISK

K Number: K960996 · Decision Apr 18, 1996
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
243
Applicant Total
109
Review Days
37

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Basic Information

Device Name
M. CAT BUTYRATE DISK
K Number
K960996
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hardy Diagnostics
Date Received
March 12, 1996
Decision Date
April 18, 1996
Product Code
JTO
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
JTO Discs, Strips And Reagents, Microorganism Differentiation

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Other Clearances by Hardy Diagnostics

K Number Device Name
K260842 HardyDisk AST Gepotidacin 10µg (GEP10)
K253105 HardyDisk AST Cefiderocol 30µg (FDC30)
K250956 HardyDisk AST Gepotidacin 10µg (GEP10)
K250454 HardyDisk Aztreonam/Avibactam 30/20µg (AZA50)
K233534 Viral Transport Medium
K241060 HardyDisk AST Cefiderocol 30µg (FDC30)
K231568 HardyDisk AST Sulbactam/Durlobactam 10/10µg (SUD20)
K230827 HardyDisk AST Rezafungin 5µg (RZF5)
K193504 HardyDisk AST Cefiderocol 30ug (FDC30)
K192326 HardyDisk AST Lefamulin 20µg (LMU20)
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