Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K111363Substantially Equivalent

Ppx Reagent, Ppx Calibrators, Ppx Qc Material

Medica Corp., Bedford MA / Traditional, Substantially Equivalent

K111363 is the FDA 510(k) clearance record for PPX REAGENT, PPX CALIBRATORS, PPX QC MATERIAL, a class II device, cleared for Medica Corp. on under FDA product code JXN (Enzyme Immunoassay, Propoxyphene). FDA records list 56 510(k) clearances for Medica Corp., from to . As of , FDA records show no recalls naming K111363.

Clearance record

Decision date
Received
(204 days to decision)
Product code
JXN Enzyme Immunoassay, Propoxyphene
Regulation
21 CFR 862.3700
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Medica Corp. 5 Oak Park Dr., Bedford MA
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