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
K914216Substantially Equivalent

Frenta II+ Enteral Feeding Pump

Fresenius Pharma, New Brunswick NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K914216 is the FDA 510(k) clearance record for FRENTA II+ ENTERAL FEEDING PUMP, a class II device, cleared for Fresenius Pharma on under FDA product code LZH (Pump, Infusion, Enteral). FDA records list 3 510(k) clearances for Fresenius Pharma, from to . As of , FDA records show no recalls naming K914216.

Clearance record

Decision date
Received
(181 days to decision)
Product code
LZH Pump, Infusion, Enteral
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
Fresenius Pharma 120 Albany St., Suite 700, New Brunswick NJ
510(k) summary
Summary
Third party review
No

Clearances, product code LZH

Trailing 12 months
1 clearance under product code LZH 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 LZH, 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