510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K020787Substantially Equivalent

Verdict-II Propoxyphene

MEDTOX Diagnostics, Inc., Burlington NC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K020787 is the FDA 510(k) clearance record for VERDICT-II PROPOXYPHENE, a class II device, cleared for Medtox Diagnostics, Inc. on under FDA product code JXN (Enzyme Immunoassay, Propoxyphene). FDA records list 22 510(k) clearances for Medtox Diagnostics, Inc., from to . As of , FDA records show no recalls naming K020787.

Clearance record

Decision date
Received
(52 days to decision)
Product code
JXN Enzyme Immunoassay, Propoxyphene
Regulation
21 CFR 862.3700
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Medtox Diagnostics, Inc. 1238 Anthony Rd., Burlington NC
510(k) summary
Statement
Third party review
No

Clearances, product code JXN

Trailing 12 months

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

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