FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BACTIDROP ACRIDINE ORANGE

K Number: K920974 · Decision Jun 19, 1992
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
0
Applicant Total
137
Review Days
109

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Basic Information

Device Name
BACTIDROP ACRIDINE ORANGE
K Number
K920974
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1145
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Remel Co.
Date Received
March 2, 1992
Decision Date
June 19, 1992
Product Code
JFO
Advisory Committee
Clinical Chemistry
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
JFO Fluorometric, Calcium

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K960095 BACTIDROP CALCOFLUOR WHITE
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K941444 BHI AGAR WITH VANCOMYCIN
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