FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BD Nexiva™ Diffusics™ Closed IV Catheter System with BD MaxZero™ Needle-free Connector

K Number: K233529 · Decision Dec 1, 2023
Classifications
1
FEI Numbers
204
Registration Numbers
205
Same Product Code
503
Applicant Total
36
Review Days
29

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Basic Information

Device Name
BD Nexiva™ Diffusics™ Closed IV Catheter System with BD MaxZero™ Needle-free Connector
K Number
K233529
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5200
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Becton Dickinson Infusion Therapy Systems, Inc.
Date Received
November 2, 2023
Decision Date
December 1, 2023
Product Code
FOZ
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
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FOZ), ordered by most recent decision date.

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Other Clearances by Becton Dickinson Infusion Therapy Systems, Inc.

K Number Device Name
K252137 BD Insyte™ IV Catheter
K251422 BD Saf-T-Intima™ Subcutaneous Catheter System
K243403 BD Nexiva™ Closed IV Catheter System
K251155 BD Cathena™ Safety IV Catheter
K251654 BD Insyte™ Autoguard™ Shielded IV Catheter, BD Insyte™ Autoguard™ BC Shielded IV Catheter and BD Insyte™ Autoguard™ BC Pro Shielded IV Catheter
K250682 BD Nexiva™ Diffusics™ Closed IV Catheter System and BD Nexiva™ Diffusics™ Closed IV Catheter System with BD MaxZero™ Needle-free Connector
K241586 PIVO™ Pro Needle-free Blood Collection Device
K230865 PIVO™ Pro Needle-free Blood Collection Device
K231239 Nexiva™ Closed IV Catheter System with NearPort™ IV Access
K220584 BD Cathena Safety IV Catheter
Search all 36 clearances from Becton Dickinson Infusion Therapy Systems, Inc. →