FDA 510(k)

HIgH-Flo Super26皮下注射針セット

K-번호: K180843 · 2019-04-04

신청자Repro-Med Systems, Inc. Dba Rms Medical Products

결정일2019-04-04

제품 코드FPA

자문 위원회의료장비 규제 텍스트 번역 HO [원문 텍스트가 제공되지 않았기 때문에 번역할 수 없습니다. 원문 텍스트를 제공해 주시면 번역을 도와드리겠습니다.]

결정대체적으로 동일

기기 요약

HIgH-Flo Super26 Subcutaneous Needle Sets is the device name listed in this FDA 510(k) record. The listed applicant is Repro-Med Systems, Inc. Dba Rms Medical Products. It received FDA 510(k) clearance on 2019-04-04 under 510(k) number K180843. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the HIgH-Flo Super26 Subcutaneous Needle Sets?

HIgH-Flo Super26 Subcutaneous Needle Sets is a medical device that received FDA 510(k) clearance on 2019-04-04. The listed applicant is Repro-Med Systems, Inc. Dba Rms Medical Products. The 510(k) number is K180843.

When did HIgH-Flo Super26 Subcutaneous Needle Sets receive FDA 510(k) clearance?

HIgH-Flo Super26 Subcutaneous Needle Sets received FDA 510(k) clearance on 2019-04-04, under 510(k) number K180843.

Who is the listed applicant for HIgH-Flo Super26 Subcutaneous Needle Sets?

The FDA 510(k) record lists Repro-Med Systems, Inc. Dba Rms Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HIgH-Flo Super26 Subcutaneous Needle Sets?

The FDA product code for HIgH-Flo Super26 Subcutaneous Needle Sets is FPA.

Repro-Med Systems, Inc. Dba Rms Medical Products를 신청인으로 등재한 기타 기록

K162613통합된 캡추 프리덤 주사기 주입 시스템

공식 출처

FDA 데이터베이스에서 보기 →

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