Catalog Number

-

Brand Name

AP504- UV RESISTANT INFUSION SET WITH VENTED/NONVENTED DRIP CHAMBER AND NEEDLELE

Version/Model Number

12000-000-0045

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

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

K123049,K123049

Product Code

FPA

Product Code Name

Set, Administration, Intravascular

Public Device Record Key

1d30804d-888f-49e6-8418-9cfbdc00da7d

Public Version Date

June 20, 2019

Public Version Number

1

DI Record Publish Date

June 12, 2019

Package DI Number

27290109159311

Quantity per Package

20

Contains DI Package

17290109159314

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Cardboard box