Catalog Number

SO1100

Brand Name

MTP

Version/Model Number

1100

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

K830453,K830453

Product Code

FPA

Product Code Name

Set, administration, intravascular

Public Device Record Key

24637172-db18-4402-bdb7-8315f7f04f58

Public Version Date

March 11, 2019

Public Version Number

1

DI Record Publish Date

February 16, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-