FDA 510(k)

PVC 수용성 요도 캐瑟터

K-번호: K212567 · 2022-12-07

신청자Chengdu Daxan Innovative Medical Tech. Co., Ltd.

결정일2022-12-07

제품 코드EZD

자문 위원회규제 정책: medical-regulatory-v1 GU

결정대체적으로 동일

기기 요약

PVC Hydrophilic Urethral Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Chengdu Daxan Innovative Medical Tech. Co., Ltd.. It received FDA 510(k) clearance on 2022-12-07 under 510(k) number K212567. The device is classified under product code EZD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the PVC Hydrophilic Urethral Catheter?

PVC Hydrophilic Urethral Catheter is a medical device that received FDA 510(k) clearance on 2022-12-07. The listed applicant is Chengdu Daxan Innovative Medical Tech. Co., Ltd.. The 510(k) number is K212567.

When did PVC Hydrophilic Urethral Catheter receive FDA 510(k) clearance?

PVC Hydrophilic Urethral Catheter received FDA 510(k) clearance on 2022-12-07, under 510(k) number K212567.

Who is the listed applicant for PVC Hydrophilic Urethral Catheter?

The FDA 510(k) record lists Chengdu Daxan Innovative Medical Tech. Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PVC Hydrophilic Urethral Catheter?

The FDA product code for PVC Hydrophilic Urethral Catheter is EZD.

Chengdu Daxan Innovative Medical Tech. Co., Ltd.를 신청인으로 등재한 기타 기록

K243175용기성 간헐적 케테터 (TPU 케테터)

공식 출처

FDA 데이터베이스에서 보기 →

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