Catalog Number

-

Brand Name

SonoScape

Version/Model Number

HD-550Pro

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

K211882

Product Code

NWB

Product Code Name

Endoscope, Accessories, Narrow Band Spectrum

Public Device Record Key

3313a627-2a6d-411c-9509-4c2d7ec9031d

Public Version Date

April 15, 2022

Public Version Number

1

DI Record Publish Date

April 07, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-