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

A.C.T. I

K Number: K965149 · Decision Jan 22, 1997
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
110
Applicant Total
137
Review Days
30

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Basic Information

Device Name
A.C.T. I
K Number
K965149
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2390
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Remel Co.
Date Received
December 23, 1996
Decision Date
January 22, 1997
Product Code
JSM
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
JSM Culture Media, Non-Propagating Transport

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K936021 BACTICARD STREP
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