FDA 510(k)

ProMedTek Model C1400 Shortwave Diathermy Device

K-번호: K162240 · 2016-11-17

결정일2016-11-17

제품 코드IMJ

자문 위원회PM

결정Substantially Equivalent

기기 요약

ProMedTek Model C1400 Shortwave Diathermy Device is the device name listed in this FDA 510(k) record. The listed applicant is Promedtek, Inc.. It received FDA 510(k) clearance on 2016-11-17 under 510(k) number K162240. 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 ProMedTek Model C1400 Shortwave Diathermy Device?

ProMedTek Model C1400 Shortwave Diathermy Device is a medical device that received FDA 510(k) clearance on 2016-11-17. The listed applicant is Promedtek, Inc.. The 510(k) number is K162240.

When did ProMedTek Model C1400 Shortwave Diathermy Device receive FDA 510(k) clearance?

ProMedTek Model C1400 Shortwave Diathermy Device received FDA 510(k) clearance on 2016-11-17, under 510(k) number K162240.

Who is the listed applicant for ProMedTek Model C1400 Shortwave Diathermy Device?

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

What is the FDA product code for ProMedTek Model C1400 Shortwave Diathermy Device?

The FDA product code for ProMedTek Model C1400 Shortwave Diathermy Device is IMJ.

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ProMedTek Model C1400 Shortwave Diathermy Device

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: IMJ)

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