FDA 510(k)

Transem and EchoGen Embryo Transfer Catheters

Número K: K161547 · 2017-03-09

Data da decisão2017-03-09

Código do produtoMQF

Comité consultivoOB

DecisãoSubstantially Equivalent

Resumo do dispositivo

Transem and EchoGen Embryo Transfer Catheters is the device name listed in this FDA 510(k) record. The listed applicant is Origio A/S. It received FDA 510(k) clearance on 2017-03-09 under 510(k) number K161547. The device is classified under product code MQF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Transem and EchoGen Embryo Transfer Catheters?

Transem and EchoGen Embryo Transfer Catheters is a medical device that received FDA 510(k) clearance on 2017-03-09. The listed applicant is Origio A/S. The 510(k) number is K161547.

When did Transem and EchoGen Embryo Transfer Catheters receive FDA 510(k) clearance?

Transem and EchoGen Embryo Transfer Catheters received FDA 510(k) clearance on 2017-03-09, under 510(k) number K161547.

Who is the listed applicant for Transem and EchoGen Embryo Transfer Catheters?

The FDA 510(k) record lists Origio A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Transem and EchoGen Embryo Transfer Catheters?

The FDA product code for Transem and EchoGen Embryo Transfer Catheters is MQF.

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