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

Disposable Sterile Needle

K Number: K172938 · Decision Jun 14, 2018
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
15
Review Days
261

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Disposable Sterile Needle
K Number
K172938
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Jiangsu Caina Medical Co.,Ltd
Date Received
September 26, 2017
Decision Date
June 14, 2018
Product Code
FMI
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
FMI Needle, Hypodermic, Single Lumen

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FMI), ordered by most recent decision date.

View all

Other Clearances by Jiangsu Caina Medical Co.,Ltd

K Number Device Name
K232781 Safety Sliding Blood Collection Set
K233190 ENFit Adaptor
K230635 Pen Needle
K220184 Pump Alignment Syringe
K211593 Enteral Pump Syringe
K210217 Needleless Connector
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
Search all 15 clearances from Jiangsu Caina Medical Co.,Ltd →