Catalog Number

-

Brand Name

S-SCORT® lll

Version/Model Number

74000

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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"

Yes

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

JCX

Product Code Name

Apparatus, Suction, Ward Use, Portable, Ac-Powered

Public Device Record Key

0cced171-e592-43b1-b9df-301217018441

Public Version Date

August 23, 2019

Public Version Number

4

DI Record Publish Date

February 13, 2017

Package DI Number

B245740001

Quantity per Package

1

Contains DI Package

B245740000

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton