Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K012107Substantially Equivalent

Livesure Phenecycline (Pcp) Screen Tests

Pan Probe Biotech, Inc., San Diego CA / Traditional, Substantially Equivalent

K012107 is the FDA 510(k) clearance record for LIVESURE PHENECYCLINE (PCP) SCREEN TESTS, cleared for Pan Probe Biotech, Inc. on under FDA product code LCM (Enzyme Immunoassay, Phencyclidine). FDA records list 10 510(k) clearances for Pan Probe Biotech, Inc., from to . As of , FDA records show no recalls naming K012107.

Clearance record

Decision date
Received
(15 days to decision)
Product code
LCM Enzyme Immunoassay, Phencyclidine
Device class
Unclassified
Review panel
Unknown
Applicant
Pan Probe Biotech, Inc. 8515 Arjons Dr., Suite A, San Diego CA
510(k) summary
Summary
Third party review
Yes

Clearances, product code LCM

Trailing 12 months

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

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