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

Promisemed X-Safety Pen Needle

K Number: K220129 · Decision Sep 19, 2022
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
35
Review Days
244

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Basic Information

Device Name
Promisemed X-Safety Pen Needle
K Number
K220129
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Promisemed Hangzhou Meditech Co., Ltd.
Date Received
January 18, 2022
Decision Date
September 19, 2022
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

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Other Clearances by Promisemed Hangzhou Meditech Co., Ltd.

K Number Device Name
K261196 Promisemed VeriEcto Automatic Biopsy Needles
K261045 Verifine Safety Lancets
K254273 Verisafe Safety Sterile Needles (SSN)
K250192 Verisafe Safety Retractable Insulin Syringes
K250961 Blood collection tube holders
K251138 Promisemed Safety Huber Needles
K243332 Promisemed Safety Huber Needles
K243806 Safety Winged Blood Collection Sets
K240675 Endoscopic Injection Needles
K242632 Verifine® Pen Needles
Search all 35 clearances from Promisemed Hangzhou Meditech Co., Ltd. →