Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle (K222852)
Description
Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle by Nipro Medical Corporation, an FDA 510(k) cleared general hospital device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K222852
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. Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle (K222852) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K162081 | BD 1ml Luer-lok Hypodermic Syringe, BD 1 mL Luer-Lok Hypode... | Becton, Dickinson and Company | 2016 |
Trace the full predicate network for K222852
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.