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

SAF FIXATIVE

K Number: K905120 · Decision Dec 17, 1990
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
62
Applicant Total
4
Review Days
33

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Basic Information

Device Name
SAF FIXATIVE
K Number
K905120
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2900
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Gibson Laboratories, Inc.
Date Received
November 14, 1990
Decision Date
December 17, 1990
Product Code
LIO
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
LIO Device, Specimen Collection

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K Number Device Name
K955826 GIBSON ID-M. CAT.
K953247 GIBSON ID A.E. TEST
K904773 P AND T MEDIUM