Catalog Number

-

Brand Name

SICAT FUNCTION

Version/Model Number

V2.0.40

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

K133320

Product Code

LLZ

Product Code Name

System, Image Processing, Radiological

Public Device Record Key

35473956-1a1d-465a-a663-2eb9cf5e97e7

Public Version Date

January 20, 2022

Public Version Number

1

DI Record Publish Date

January 12, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-