LDV((Low Dead Volume )Syringe— 510(k) K220083

Substantially Equivalent

Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd.

FDA 510(k) clearance K220083 for LDV((Low Dead Volume )Syringe, Substantially Equivalent on 2022-05-25. Applicant: Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd.. Device class: 2.

Clearance details

Applicant
Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd.
Product code
Code QNQ
Device class
Class 2
Regulation
21 CFR 880.5860
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Anqing, CN
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