Catalog Number

8010013-01

Brand Name

D-SPECT Refurbished

Version/Model Number

D-SPECT 004

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

K161740

Product Code

KPS

Product Code Name

System, Tomography, Computed, Emission

Public Device Record Key

2198db02-7b95-4fe6-8ab4-72c7ffd1356c

Public Version Date

December 21, 2020

Public Version Number

2

DI Record Publish Date

August 26, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-