510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K012907Substantially Equivalent

Liquispx Liquid Saliva or Unrine Drug of Abuse Control

Clinical Controls, Inc., Hawaiian Gardens CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K012907 is the FDA 510(k) clearance record for LIQUISPX LIQUID SALIVA OR UNRINE DRUG OF ABUSE CONTROL, a class I device, cleared for Clinical Controls on under FDA product code DIF (Drug Mixture Control Materials). FDA records list 18 510(k) clearances for Clinical Controls, from to . As of , FDA records show no recalls naming K012907.

Clearance record

Decision date
Received
(30 days to decision)
Product code
DIF Drug Mixture Control Materials
Regulation
21 CFR 862.3280
Device class
Class I
Review panel
Clinical Toxicology
Applicant
Clinical Controls 12038 Centralia Rd., Hawaiian Gardens CA
510(k) summary
Statement
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