510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K030649Substantially Equivalent

Dri Cotinine Eia Assay

Microgenics Corporation, Fremont Blvd. CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K030649 is the FDA 510(k) clearance record for DRI COTININE EIA ASSAY, a class I device, cleared for Microgenics Corp. on under FDA product code MRS (Test System, Nicotine, Cotinine, Metabolites). FDA records list 128 510(k) clearances for Microgenics Corp., from to . As of , FDA records show no recalls naming K030649.

Clearance record

Decision date
Received
(83 days to decision)
Product code
MRS Test System, Nicotine, Cotinine, Metabolites
Regulation
21 CFR 862.3220
Device class
Class I
Review panel
Clinical Toxicology
Applicant
Microgenics Corp. 46360 Fremont Blvd., Fremont Blvd. CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MRS

Trailing 12 months

FDA records hold no clearances under product code MRS in the trailing twelve months.

FDA records show no clearances under product code MRS in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MRS, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260