FDA 510(k)

AMSure Enteral Feeding Pump

Número K: K220230 · 2022-11-10

Data da decisão2022-11-10

Código do produtoLZH

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

AMSure Enteral Feeding Pump is the device name listed in this FDA 510(k) record. The listed applicant is Amsino International, Inc.. It received FDA 510(k) clearance on 2022-11-10 under 510(k) number K220230. The device is classified under product code LZH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the AMSure Enteral Feeding Pump?

AMSure Enteral Feeding Pump is a medical device that received FDA 510(k) clearance on 2022-11-10. The listed applicant is Amsino International, Inc.. The 510(k) number is K220230.

When did AMSure Enteral Feeding Pump receive FDA 510(k) clearance?

AMSure Enteral Feeding Pump received FDA 510(k) clearance on 2022-11-10, under 510(k) number K220230.

Who is the listed applicant for AMSure Enteral Feeding Pump?

The FDA 510(k) record lists Amsino International, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMSure Enteral Feeding Pump?

The FDA product code for AMSure Enteral Feeding Pump is LZH.

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Outros registros que listam Amsino International, Inc. como candidato(a)

K252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)K220267AMSafe NeuFlo Needleless Connector K213522AMSafe Pre-Filled Normal Saline Flush Syringe K200051PUGGLE Enteral Feeding Pump and Feeding Set K183473AMSafe(R) Pre-Filled Normal Saline Flush Syringe K181445AMSure Hydrophilic Intermittent Catheter

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Fonte oficial

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