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
K030739Substantially Equivalent

Infusion Dynamics (Id) Power Infuser, Model M100b-3A with Blood Cartridge

Infusion Dynamics, Inc., Frederick MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K030739 is the FDA 510(k) clearance record for INFUSION DYNAMICS (ID) POWER INFUSER, MODEL M100B-3A WITH BLOOD CARTRIDGE, a class II device, cleared for Infusion Dynamics, Inc. on under FDA product code FRN (Pump, Infusion). FDA records list 3 510(k) clearances for Infusion Dynamics, Inc., from to . As of , FDA records show one recall naming K030739.

Clearance record

Decision date
Received
(310 days to decision)
Product code
FRN Pump, Infusion
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
Infusion Dynamics, Inc. 5340 Spectrum Dr., Suite N, Frederick MD
510(k) summary
Statement
Third party review
No

Clearances, product code FRN

Trailing 12 months
2 clearances under product code FRN 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 FRN, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260