Catalog Number

-

Brand Name

Discovery 630

Version/Model Number

H3100JY

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

K111445

Product Code

KPS

Product Code Name

System, tomography, computed, emission

Public Device Record Key

5ef14294-ebc7-46ac-b7e0-ac383bbd50dc

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

May 13, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-