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

Emit II Plus Cocaine Metabolite Assay

K Number: K170293 · Decision Oct 25, 2017
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
144
Applicant Total
152
Review Days
267

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Emit II Plus Cocaine Metabolite Assay
K Number
K170293
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3250
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens Healthcare Diagnostics, Inc.
Date Received
January 31, 2017
Decision Date
October 25, 2017
Product Code
DIO
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
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DIO), ordered by most recent decision date.

View all

Other Clearances by Siemens Healthcare Diagnostics, Inc.

K Number Device Name
K251998 Atellica CH Diazo Total Bilirubin (D_TBil)
K251543 Atellica® IM TSH3-Ultra II (TSH3ULII)
K251630 Atellica IM Total PSA II (tPSAII)
K250816 ADVIA Centaur Anti-Thyroglobulin II (aTgII)
K250250 ADVIA Centaur Anti-Thyroid Peroxidase II
K242981 Atellica IM Thyroglobulin (Tg)
K242685 Atellica® CH Creatinine_3 (Crea3)
K241800 Atellica® CH HDL Cholesterol (HDLC)& Atellica® CH LDL Cholesterol (LDLC)
K241165 Atellica® IM High-Sensitivity Troponin I (TnIH)
K233050 ADVIA Centaur® TSH3-Ultra II (TSH3ULII)
Search all 152 clearances from Siemens Healthcare Diagnostics, Inc. →