FDA 510(k)

Disposable Endoscopic Hemoclip

K-번호: K222146 · 2023-03-28

신청자Jiangsu Vedkang Medical Science and Technology Co., Ltd.

결정일2023-03-28

제품 코드PKL

자문 위원회GU

결정Substantially Equivalent

기기 요약

Disposable Endoscopic Hemoclip is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Vedkang Medical Science and Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-03-28 under 510(k) number K222146. The device is classified under product code PKL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Disposable Endoscopic Hemoclip?

Disposable Endoscopic Hemoclip is a medical device that received FDA 510(k) clearance on 2023-03-28. The listed applicant is Jiangsu Vedkang Medical Science and Technology Co., Ltd.. The 510(k) number is K222146.

When did Disposable Endoscopic Hemoclip receive FDA 510(k) clearance?

Disposable Endoscopic Hemoclip received FDA 510(k) clearance on 2023-03-28, under 510(k) number K222146.

Who is the listed applicant for Disposable Endoscopic Hemoclip?

The FDA 510(k) record lists Jiangsu Vedkang Medical Science and Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Endoscopic Hemoclip?

The FDA product code for Disposable Endoscopic Hemoclip is PKL.

Jiangsu Vedkang Medical Science and Technology Co., Ltd.를 신청인으로 등재한 기타 기록

K232825Disposable Sphincterotome K232752Stone Extraction Balloon (VDK-BAL-23-11/13/15-B,VDK-BAL-23-15/18/20-B,VDK-BAL-23-9/12/15-B,VDK-BAL-23-10/13/16-B,VDK-BAL-23-8.5/11.5/15-B,VDK-BAL-23-12/15/18-B,VDK-BAL-23-11/13/15-C,VDK-BAL-23-15/18/20-C,VDK-BAL-23-9/12/15-C,VDK-BAL-23-10/13/16-C,VDK-BAL-23-8.5/11.5/15-C,VDK-BAL-23-12/15/18-C)K232245VedDilator ^TM (3-Stage Balloon Dilation Catheter)K230598Stone Extraction Baskets K220089Disposable Polyp Snare K213914Injection Needle

7개 장치 모두 보기 →

공식 출처

FDA 데이터베이스에서 보기 →

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