510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K002776Substantially Equivalent

Modification to Profile -II

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

K002776 is the FDA 510(k) clearance record for MODIFICATION TO PROFILE -II, cleared for Medtox Diagnostics, Inc. on under FDA product code LCM (Enzyme Immunoassay, Phencyclidine). FDA records list 22 510(k) clearances for Medtox Diagnostics, Inc., from to . As of , FDA records show no recalls naming K002776.

Clearance record

Decision date
Received
(22 days to decision)
Product code
LCM Enzyme Immunoassay, Phencyclidine
Device class
Unclassified
Review panel
Unknown
Applicant
Medtox Diagnostics, Inc. 1238 Anthony Rd., Burlington NC
510(k) summary
Statement
Third party review
No

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