FDA 510(k)

3.0T Air MP M, 3.0T Air MP L

Número K: K182504 · 2018-10-12

RequerenteGe Healthcare Coils (Usa Instruments, Inc.)

Data da decisão2018-10-12

Código do produtoMOS

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

3.0T Air MP M, 3.0T Air MP L is the device name listed in this FDA 510(k) record. The listed applicant is Ge Healthcare Coils (Usa Instruments, Inc.). It received FDA 510(k) clearance on 2018-10-12 under 510(k) number K182504. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the 3.0T Air MP M, 3.0T Air MP L?

3.0T Air MP M, 3.0T Air MP L is a medical device that received FDA 510(k) clearance on 2018-10-12. The listed applicant is Ge Healthcare Coils (Usa Instruments, Inc.). The 510(k) number is K182504.

When did 3.0T Air MP M, 3.0T Air MP L receive FDA 510(k) clearance?

3.0T Air MP M, 3.0T Air MP L received FDA 510(k) clearance on 2018-10-12, under 510(k) number K182504.

Who is the listed applicant for 3.0T Air MP M, 3.0T Air MP L?

The FDA 510(k) record lists Ge Healthcare Coils (Usa Instruments, Inc.) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3.0T Air MP M, 3.0T Air MP L?

The FDA product code for 3.0T Air MP M, 3.0T Air MP L is MOS.

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Fonte oficial

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