510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K003476Substantially Equivalent

Mps Acacia Pain Kit

Mps Acacia, Brea CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K003476 is the FDA 510(k) clearance record for MPS ACACIA PAIN KIT, a class II device, cleared for Mps Acacia on under FDA product code MEB (Pump, Infusion, Elastomeric). FDA records list 7 510(k) clearances for Mps Acacia, from to . As of , FDA records show no recalls naming K003476.

Clearance record

Decision date
Received
(64 days to decision)
Product code
MEB Pump, Infusion, Elastomeric
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
Mps Acacia 499 Nibus St., Suite E, Brea CA
510(k) summary
Summary
Third party review
No

Clearances, product code MEB

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