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

STATUS DS OXY

K Number: K130650 · Decision Feb 26, 2014
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
214
Applicant Total
72
Review Days
352

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Basic Information

Device Name
STATUS DS OXY
K Number
K130650
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3650
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Princeton BioMeditech Corp.
Date Received
March 11, 2013
Decision Date
February 26, 2014
Product Code
DJG
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
DJG Enzyme Immunoassay, Opiates

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K062575 MODIFICATION TO: ACCUSIGN RC DOA 10 (MET/OPI/COC/THC/PCP/BZO/BAR/MTD/TCA/AMP
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