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

DRI PRIMIDONE CALIBRATORS

K Number: K023780 · Decision Feb 10, 2003
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
122
Applicant Total
107
Review Days
90

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Basic Information

Device Name
DRI PRIMIDONE CALIBRATORS
K Number
K023780
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3200
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Microgenics Corp.
Date Received
November 12, 2002
Decision Date
February 10, 2003
Product Code
DLJ
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
DLJ Calibrators, Drug Specific

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K110616 THERMO SCIENTIFIC MAS OMNI-IMMUNE, MAS OMNI IMMUNE PRO
K101742 THERMO SCIENTIFIC CEDIA COCAINE OFT ASSAY
K101744 THERMO SCIENTIFIC CEDIA CANNABINOIDS OFT ASSAY
K101752 THERMO SCIENTIFIC CEDIA MULTI-DRUG OFT CALIBRATORS
K101746 THERMO SCIENTIFIC CEDIA PHENCYCLIDINE (PCP) OFT ASSAY
K101753 THERMO SCIENTIFIC CEDIA METHAMPHETAMINE OFT ASSAY
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