FDA 510(k)

Megapulse III Shortwave Diathermy

K-번호: K153456 · 2016-06-14

결정일2016-06-14

제품 코드IMJ

자문 위원회PM

결정Substantially Equivalent

기기 요약

Megapulse III Shortwave Diathermy is the device name listed in this FDA 510(k) record. The listed applicant is Accelerated Care Plus. It received FDA 510(k) clearance on 2016-06-14 under 510(k) number K153456. The device is classified under product code IMJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Megapulse III Shortwave Diathermy?

Megapulse III Shortwave Diathermy is a medical device that received FDA 510(k) clearance on 2016-06-14. The listed applicant is Accelerated Care Plus. The 510(k) number is K153456.

When did Megapulse III Shortwave Diathermy receive FDA 510(k) clearance?

Megapulse III Shortwave Diathermy received FDA 510(k) clearance on 2016-06-14, under 510(k) number K153456.

Who is the listed applicant for Megapulse III Shortwave Diathermy?

The FDA 510(k) record lists Accelerated Care Plus as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Megapulse III Shortwave Diathermy?

The FDA product code for Megapulse III Shortwave Diathermy is IMJ.

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Megapulse III Shortwave Diathermy

기기 요약

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관련 임상시험

관련 기기 (코드: IMJ)

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