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

SEFRIA™ Hydrocodone Oral Fluid

K Number: K252520 · Decision Sep 11, 2025
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
214
Applicant Total
50
Review Days
31

Basic Information

Device Name
SEFRIA™ Hydrocodone Oral Fluid
K Number
K252520
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3650
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Immunalysis Corporation
Date Received
August 11, 2025
Decision Date
September 11, 2025
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

Similar 510(k) Clearances

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

View all

Other Clearances by Immunalysis Corporation

K Number Device Name
K232898 Quantisal™ Oral Fluid Collection Device
K223781 Quantisal™ II Oral Fluid Collection Device
K203647 SEFRIA Methamphetamine Oral Fluid Enzyme Immunoassay
K203564 SEFRIA Oxycodone Oral Fluid Enzyme Immunoassay
K203489 SEFRIA PCP Oral Fluid Enzyme Immunoassay
K200801 Quantisal Oral Fluid Collection Device
K190397 Immunalysis Carisoprodol Metabolite / Meprobamate Urine HEIA
K183048 Quantisal II Oral Fluid Collection Device
K181135 Immunalysis SEFRIA PCP Oral Fluid Enzyme Immunoassay
K181553 Immunalysis Ethyl Alcohol Enzyme Assay
Search all 50 clearances from Immunalysis Corporation →