Compat Go Enteral Feeding Pump and Administration Sets

FDA 510(k) K060316 · Fresenius Kabi Deutschland GmbH

Substantially Equivalent

510(k) numberK060316

Submission

Device name
Compat Go Enteral Feeding Pump and Administration Sets
Applicant
Fresenius Kabi Deutschland GmbH
Bad Homburg, DE
Received
February 8, 2006
Decision date
June 23, 2006
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
LZH – Pump, Infusion, Enteral
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5725
Specialty
General Hospital

Other 510(k)s with product code LZH

510(k)DeviceApplicantDecision
K253558Luminoah FLOW™ Enteral Nutrition SystemLZH · Traditional Luminoah04/20/2026SE
K232205Vesco Q™ Enteral Feeding Pump; Vesco Q™ 500mL Bag Feed Set; Vesco Q™ 1000mL Bag Feed…LZH · Traditional Vesco Medical, LLC10/23/2023SE
K221603Kangaroo OMNI™ Enteral Feeding Pump (385400 );Kangaroo OMNI™ Feeding Set 500ml (B5FD…LZH · Traditional Cardinal Health, LLC12/20/2022SE
K220230AMSure Enteral Feeding PumpLZH · Traditional Amsino International, Inc.11/10/2022SE
K200051PUGGLE Enteral Feeding Pump and Feeding SetLZH · Traditional Amsino International, Inc.09/25/2020SE
K153074Kangaroo Connect Enteral Feeding Pump with Kangaroo Connect Feeding Sets, Kangaroo…LZH · Traditional Covidien07/06/2016SE
K143263Kangaroo Connect Enteral Feeding Pump with Kangaroo Connect Feeding SetsLZH · Traditional Covidien05/29/2015SE
K141479Kangaroo Enteral Feeding Set with Enfit ConnectorsLZH · Traditional Covidien12/23/2014SE
K131154Enteralite Infinity Spike Enteral Delivery Set; Enteralite Infinity 500 ML Bag Enteral…LZH · Special Zevex, Inc.02/12/2014SE
K111381Medi-Sis Syringe Infusion SystemLZH · Traditional Acacia, Inc.01/13/2012SE

Questions and answers

When was Compat Go Enteral Feeding Pump and Administration Sets cleared by the FDA?

Compat Go Enteral Feeding Pump and Administration Sets (K060316) received a 510(k) decision of Substantially Equivalent on June 23, 2006, 135 days after the submission was received.

What is the product code of K060316?

The FDA product code is LZH – Pump, Infusion, Enteral, a Class II (moderate risk) device regulated under 21 CFR 880.5725.