Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K964844Substantially Equivalent

Conmed: Stat 2 and Stat 2 Pumpette Extension Sets and Masterflow and Masterflow Pumpette Primary Sets

Conmedcorp, Utica NY / Traditional, Substantially Equivalent

K964844 is the FDA 510(k) clearance record for CONMED: STAT 2 AND STAT 2 PUMPETTE EXTENSION SETS AND MASTERFLOW AND MASTERFLOW PUMPETTE PRIMARY SETS, a class II device, cleared for Conmedcorp on under FDA product code FPA (Set, Administration, Intravascular). FDA records list 92 510(k) clearances for Conmedcorp, from to . As of , FDA records show 12 recalls naming K964844.

Clearance record

Decision date
Received
(111 days to decision)
Product code
FPA Set, Administration, Intravascular
Regulation
21 CFR 880.5440
Device class
Class II
Review panel
General Hospital
Applicant
Conmedcorp 310 Broad St., Utica NY
510(k) summary
Statement
Third party review
No

Clearances, product code FPA

Trailing 12 months
5 clearances under product code FPA in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FPA, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20260
April 20260
May 20261
June 20261
July 20260
August 20260
September 20261
October 20260