Catalog Number

391662

Brand Name

BD Neoflon Pro Safety Safety IV Catheter

Version/Model Number

391662

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K172506,K172506

Product Code

FOZ

Product Code Name

Catheter, intravascular, therapeutic, short-term less than 30 days

Public Device Record Key

a1aa2c9c-1482-4910-b548-8dc59ebc3e61

Public Version Date

November 22, 2018

Public Version Number

1

DI Record Publish Date

October 22, 2018

Package DI Number

30382903916628

Quantity per Package

30

Contains DI Package

00382903916627

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shelfpack