510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K012131Substantially Equivalent

Livesure Benzodiazepines Screen Tests

Pan Probe Biotech, Inc., San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K012131 is the FDA 510(k) clearance record for LIVESURE BENZODIAZEPINES SCREEN TESTS, a class II device, cleared for Pan Probe Biotech, Inc. on under FDA product code JXM (Enzyme Immunoassay, Benzodiazepine). FDA records list 10 510(k) clearances for Pan Probe Biotech, Inc., from to . As of , FDA records show no recalls naming K012131.

Clearance record

Decision date
Received
(11 days to decision)
Product code
JXM Enzyme Immunoassay, Benzodiazepine
Regulation
21 CFR 862.3170
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Pan Probe Biotech, Inc. 8515 Arjons Dr., Suite A, San Diego CA
510(k) summary
Summary
Third party review
Yes

Clearances, product code JXM

Trailing 12 months

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

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