Promisemed Safety Huber Needle

FDA 510(k) K230715 · Promisemed Hangzhou Meditech Co., Ltd.

Substantially Equivalent

510(k) numberK230715

Submission

Device name
Promisemed Safety Huber Needle
Applicant
Promisemed Hangzhou Meditech Co., Ltd.
Hangzhou City, CN
Received
March 15, 2023
Decision date
June 8, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
PTI – Non-Coring (Huber) Needle
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5570
Specialty
General Hospital

The non-coring needle (Huber) is utilized to gain access into a subcutaneous implanted intravascular infusion port but can also be used to access other non-vascular implanted devices with similar septums.

Other 510(k)s with product code PTI

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K252355K-SHIELD Advantage PORT ACCESS INFUSION SET With High Pressure TubingPTI · Traditional Sb-Kawasumi Laboratories, Inc.11/26/2025SE
K251138Promisemed Safety Huber NeedlesPTI · Special Promisemed Hangzhou Meditech Co., Ltd.05/13/2025SE
K243332Promisemed Safety Huber NeedlesPTI · Special Promisemed Hangzhou Meditech Co., Ltd.03/14/2025SE
K241353PowerLoc™ Max Power Injectable Infusion Set; SafeStep™ Huber Needle SetPTI · Traditional Bard Access Systems, Inc.11/27/2024SE
K213823Intera Refill KitPTI · Special Intera Oncology, Inc.03/16/2022SE
K211121Intera Non-coring (Huber) Refill Needles, Intera Non-coring (Huber) Special bolus…PTI · Traditional Intera Oncology, Inc.10/14/2021SE
K200463Huber Needle Infusion Set, Safety Huber Needle Infusion SetPTI · Traditional Jiangsu Caina Medical Co.,Ltd04/07/2021SE
K170881ISP Safety Huber Needle Infusion SetPTI · Traditional Infusion Safety Products, Inc.12/14/2017SE
K170897Surecan Safety II Needle, Surecan Safety II Needle, Surecan Safety II Needle with…PTI · Traditional B.Braun Medical, Inc.11/03/2017SE
K171735PowerLoc MAX Power-Injectable Infusion Set and SafeStep Huber Needle SetPTI · Special C.R. Bard, Inc.08/08/2017SE

More from C.R. Bard, Inc.

510(k)DeviceDecision
K261719Promisemed X-Safety Pen NeedleFMI · Special 08/25/2026SE
K261196Promisemed VeriEcto Automatic Biopsy NeedlesKNW · Special 05/12/2026SE
K261045Verifine Safety LancetsFMK · Special 05/01/2026SE
K254273Verisafe Safety Sterile Needles (SSN)FMI · Special 04/16/2026SE
K250192Verisafe Safety Retractable Insulin SyringesFMF · Traditional 12/10/2025SE
K250961Blood collection tube holdersJKA · Traditional 06/04/2025SE
K251138Promisemed Safety Huber NeedlesPTI · Special 05/13/2025SE
K243332Promisemed Safety Huber NeedlesPTI · Special 03/14/2025SE
K243806Safety Winged Blood Collection SetsFMI · Special 01/10/2025SE
K240675Endoscopic Injection NeedlesFBK · Traditional 10/04/2024SE

Questions and answers

When was Promisemed Safety Huber Needle cleared by the FDA?

Promisemed Safety Huber Needle (K230715) received a 510(k) decision of Substantially Equivalent on June 8, 2023, 85 days after the submission was received.

What is the product code of K230715?

The FDA product code is PTI – Non-Coring (Huber) Needle, a Class II (moderate risk) device regulated under 21 CFR 880.5570.