AMSafe Sure-Lok Needle-Free Connector

FDA 510(k) K173665 · Amsino International, Inc.

Substantially Equivalent

510(k) numberK173665

Submission

Device name
AMSafe Sure-Lok Needle-Free Connector
Applicant
Amsino International, Inc.
Pomona, CA, US
Received
November 29, 2017
Decision date
September 5, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FPA – Set, Administration, Intravascular
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

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K252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072…FPA · Traditional Amsino International, Inc.05/04/2026SE
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More from B.Braun Medical, Inc.

510(k)DeviceDecision
K252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072…FPA · Traditional 05/04/2026SE
K220230AMSure Enteral Feeding PumpLZH · Traditional 11/10/2022SE
K220267AMSafe NeuFlo Needleless ConnectorFPA · Traditional 10/07/2022SE
K213522AMSafe Pre-Filled Normal Saline Flush SyringeNGT · Traditional 03/22/2022SE
K200051PUGGLE Enteral Feeding Pump and Feeding SetLZH · Traditional 09/25/2020SE
K183473AMSafe(R) Pre-Filled Normal Saline Flush SyringeNGT · Traditional 07/12/2019SE
K181445AMSure Hydrophilic Intermittent CatheterEZD · Traditional 10/01/2018SE
K181423AMSure Sterile Water, and Sterile Normal Saline for Wound FlushFRO · Traditional 09/07/2018SE
K181814AMSure Pre-filled Syringe for Balloon Inflation with Sterile WaterEZL · Traditional 09/04/2018SE
K171857AMSure® Enteral Feeding Syringe with ENFit TipPNR · Traditional 03/30/2018SE

Questions and answers

When was AMSafe Sure-Lok Needle-Free Connector cleared by the FDA?

AMSafe Sure-Lok Needle-Free Connector (K173665) received a 510(k) decision of Substantially Equivalent on September 5, 2018, 280 days after the submission was received.

What is the product code of K173665?

The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.