510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K060417Substantially Equivalent

Modification to Quantimetrix Urine Drugs of Abuse Control

Quantimetrix Corp., Redondo Beach CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K060417 is the FDA 510(k) clearance record for MODIFICATION TO QUANTIMETRIX URINE DRUGS OF ABUSE CONTROL, a class I device, cleared for Quantimetrix Corp. on under FDA product code DIF (Drug Mixture Control Materials). FDA records list 39 510(k) clearances for Quantimetrix Corp., from to . As of , FDA records show no recalls naming K060417.

Clearance record

Decision date
Received
(32 days to decision)
Product code
DIF Drug Mixture Control Materials
Regulation
21 CFR 862.3280
Device class
Class I
Review panel
Clinical Toxicology
Applicant
Quantimetrix Corp. 2005 Manhattan Beach Blvd., Redondo Beach CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DIF

Trailing 12 months

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

FDA records show no clearances under product code DIF in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DIF, 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