Catalog Number

-

Brand Name

B500 SERIES

Version/Model Number

B505-1017

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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"

Yes

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

-

Product Code

DQA

Product Code Name

Oximeter

Public Device Record Key

eb28b68b-25f8-47bb-aba1-fbad3b70bab9

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 15, 2017

Package DI Number

B505101703

Quantity per Package

1

Contains DI Package

B5051017

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX