FDA 510(k)

Patient Positioning System

K-번호: K170502 · 2017-04-13

결정일2017-04-13

제품 코드JAI

자문 위원회RA

결정Substantially Equivalent

기기 요약

Patient Positioning System is the device name listed in this FDA 510(k) record. The listed applicant is Forte Automation Systems, Inc.. It received FDA 510(k) clearance on 2017-04-13 under 510(k) number K170502. The device is classified under product code JAI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Patient Positioning System?

Patient Positioning System is a medical device that received FDA 510(k) clearance on 2017-04-13. The listed applicant is Forte Automation Systems, Inc.. The 510(k) number is K170502.

When did Patient Positioning System receive FDA 510(k) clearance?

Patient Positioning System received FDA 510(k) clearance on 2017-04-13, under 510(k) number K170502.

Who is the listed applicant for Patient Positioning System?

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

What is the FDA product code for Patient Positioning System?

The FDA product code for Patient Positioning System is JAI.

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Patient Positioning System

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관련 임상시험

관련 기기 (코드: JAI)

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