Catalog Number

-

Brand Name

Hisense

Version/Model Number

HMD5G21S

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

K221567

Product Code

PGY

Product Code Name

Display, Diagnostic Radiology

Public Device Record Key

72384c3e-d4b9-449e-b739-1d4eb167428c

Public Version Date

October 24, 2022

Public Version Number

2

DI Record Publish Date

September 13, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-