510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K042500Substantially Equivalent

Duopross Syringes

Duopross Meditech Corporation, Albuquerque NM / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K042500 is the FDA 510(k) clearance record for DUOPROSS SYRINGES, a class II device, cleared for Duopross Meditech Corporation on under FDA product code FMF (Syringe, Piston). FDA records list 2 510(k) clearances for Duopross Meditech Corporation, from to . As of , FDA records show no recalls naming K042500.

Clearance record

Decision date
Received
(161 days to decision)
Product code
FMF Syringe, Piston
Regulation
21 CFR 880.5860
Device class
Class II
Review panel
General Hospital
Applicant
Duopross Meditech Corporation 12200 Academy Rd. NE, # 931, Albuquerque NM
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FMF

Trailing 12 months
14 clearances under product code FMF in the twelve months to October 2026, December 2025 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code FMF, trailing twelve months
MonthClearances
November 20251
December 20254
January 20260
February 20261
March 20260
April 20261
May 20261
June 20262
July 20261
August 20263
September 20260
October 20260