Catalog Number

RT-5100-05

Brand Name

Symphony™

Version/Model Number

RT-5100-05

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

K160627

Product Code

FRZ

Product Code Name

Device, Patient Transfer, Powered

Public Device Record Key

48b382ea-1bf1-4807-856c-710843ec1797

Public Version Date

July 06, 2018

Public Version Number

2

DI Record Publish Date

April 18, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-