Catalog Number

-

Brand Name

DISCOVERY

Version/Model Number

IGS 7 001

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"

-

For Single-Use

-

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

K122457,K181403,K133278

Product Code

IZI

Product Code Name

System, X-Ray, Angiographic

Public Device Record Key

b0ff2325-cf7f-4127-bbab-a294e05eb1fb

Public Version Date

December 06, 2018

Public Version Number

4

DI Record Publish Date

February 11, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-