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

BACTI-SWAB(TM) NPG

K Number: K912832 · Decision Aug 22, 1991
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
62
Applicant Total
137
Review Days
57

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Basic Information

Device Name
BACTI-SWAB(TM) NPG
K Number
K912832
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2900
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Remel Co.
Date Received
June 26, 1991
Decision Date
August 22, 1991
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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K965149 A.C.T. I
K960090 CALCOFLUOR WHITE STAIN KIT
K960095 BACTIDROP CALCOFLUOR WHITE
K955669 REMEL CEFEPIME 30 UG SUSCEPTIBILITY DISK
K941443 SYNERGY QUAD
K941444 BHI AGAR WITH VANCOMYCIN
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