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

BACTIDROP KOH (10%)

K Number: K920970 · Decision Jun 9, 1992
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
39
Applicant Total
137
Review Days
99

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Basic Information

Device Name
BACTIDROP KOH (10%)
K Number
K920970
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.1850
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Remel Co.
Date Received
March 2, 1992
Decision Date
June 9, 1992
Product Code
JTS
Advisory Committee
Hematology
Review Advisory Committee
PA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JTS Stains, Microbiologic

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K Number Device Name
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K965152 A.C.T. II
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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