Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K982048Substantially Equivalent

Mps Reservoir Bag

Medical Product Specialists, Brea CA / Traditional, Substantially Equivalent

K982048 is the FDA 510(k) clearance record for MPS RESERVOIR BAG, a class II device, cleared for Medical Product Specialists on under FDA product code KPE (Container, I.V.). FDA records list 4 510(k) clearances for Medical Product Specialists, from to . As of , FDA records show no recalls naming K982048.

Clearance record

Decision date
Received
(47 days to decision)
Product code
KPE Container, I.V.
Regulation
21 CFR 880.5025
Device class
Class II
Review panel
General Hospital
Applicant
Medical Product Specialists 499 Nibus St., Suite E, Brea CA
510(k) summary
Summary
Third party review
No

Clearances, product code KPE

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