Class Class II

Sofjec (K212635)

K212635 2023-02-13 Traditional
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Description

Sofjec by Hwajin Medical Co., Ltd., an FDA 510(k) cleared general hospital device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK212635
Clearance Date2023-02-13
Clearance TypeTraditional
Product CodeFMF
Regulation Number880.5860

Categories

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Predicate lineage for K212635

A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Sofjec (K212635) cites 2 predicate devices and is itself cited by 1 later device.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K190002Sterile Hypodermic Syringe for Single use, with/without nee...Shanghai Kohope Medical Devices Co....2019
K173743Greenmedi Safety Filter SyringeSang-A Frontec Co., Ltd.2019

Later devices that cite this one as their predicate

Devices that cite K212635
K numberDeviceApplicantYear
K241856Sofjec (Single use Needle); Sofjec (Single use Syringe with...Hlb Lifescience Co., Ltd.2024

Trace the full predicate network for K212635

A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.

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