Catalog Number

-

Brand Name

FORE-SIGHT ELITE

Version/Model Number

01-06-1000

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

K180003

Product Code

MUD

Product Code Name

Oximeter, Tissue Saturation

Public Device Record Key

8d0adc4d-2b26-48ea-b598-321e1f6ef15f

Public Version Date

January 14, 2019

Public Version Number

1

DI Record Publish Date

December 12, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-