FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Pump Alignment Syringe

K Number: K220184 · Decision Jul 21, 2022
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
15
Review Days
178

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Basic Information

Device Name
Pump Alignment Syringe
K Number
K220184
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Jiangsu Caina Medical Co.,Ltd
Date Received
January 24, 2022
Decision Date
July 21, 2022
Product Code
FMF
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FMF Syringe, Piston

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K200463 Huber Needle Infusion Set, Safety Huber Needle Infusion Set
K201356 Plastic LOR Syringe
K200027 Blood Collection Needle with/without Holder, Safety Blood Collection Needle with/without Holder, Luer Access Device-holder with Preattached Multiple Sample Adapter
K193022 Retractable Safety Insulin Syringe
K193526 Syringe with safety needle, Safety needle
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