Catalog Number

-

Brand Name

InfiMed Digital Imaging System, i5, RF, CCD Camera

Version/Model Number

i5 RF

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

K093066

Product Code

IZI

Product Code Name

System, X-Ray, Angiographic

Public Device Record Key

1ef857b0-6e5e-4b37-aa8a-ac4298daee2d

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

March 24, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-