510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K011011Substantially Equivalent

Livesure Morphine Screen Test

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

K011011 is the FDA 510(k) clearance record for LIVESURE MORPHINE SCREEN TEST, a class II device, cleared for Pan Probe Biotech, Inc. on under FDA product code DOE (Radioimmunoassay, Morphine (125-I), Goat Antibody Ammonium Sulfate Sep.). FDA records list 10 510(k) clearances for Pan Probe Biotech, Inc., from to . As of , FDA records show no recalls naming K011011.

Clearance record

Decision date
Received
(9 days to decision)
Product code
DOE Radioimmunoassay, Morphine (125-I), Goat Antibody Ammonium Sulfate Sep.
Regulation
21 CFR 862.3640
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 DOE

Trailing 12 months

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

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