PICO Single Use Negative Pressure Wound Therapy System

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PICO Single Use Negative Pressure Wound Therapy System is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew Medical, Ltd.. It received FDA 510(k) clearance on 2016-01-28 under 510(k) number K151436. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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What is the PICO Single Use Negative Pressure Wound Therapy System?

PICO Single Use Negative Pressure Wound Therapy System is a medical device that received FDA 510(k) clearance on 2016-01-28. The listed applicant is Smith & Nephew Medical, Ltd.. The 510(k) number is K151436.

When did PICO Single Use Negative Pressure Wound Therapy System receive FDA 510(k) clearance?

PICO Single Use Negative Pressure Wound Therapy System received FDA 510(k) clearance on 2016-01-28, under 510(k) number K151436.

Who is the listed applicant for PICO Single Use Negative Pressure Wound Therapy System?

The FDA 510(k) record lists Smith & Nephew Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PICO Single Use Negative Pressure Wound Therapy System?

The FDA product code for PICO Single Use Negative Pressure Wound Therapy System is OMP.

Smith & Nephew Medical, Ltd.를 신청인으로 등재한 기타 기록

관련 기록은 이름, 제품 코드 또는 기타 메타데이터를 사용하여 자동으로 매칭됩니다. 매칭은 검증된 임상, 과학, 기업 또는 규제 상의 관계를 입증하지 않으며, 연결된 공식 출처를 검토하시기 바랍니다.

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FDA Open API에서 수집된 데이터입니다. 가장 정확하고 공인된 정보는 항상 공식 레코드를 참조하시기 바랍니다.

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관련 임상시험

Smith & Nephew Medical, Ltd.를 신청인으로 등재한 기타 기록

관련 기기 (코드: OMP)

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