Catalog Number

FX2110X15B

Brand Name

Trilogy Evo

Version/Model Number

FX2110X15B

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

K181166

Product Code

CBK

Product Code Name

Ventilator, continuous, facility use

Public Device Record Key

b91b0c46-020a-4ec0-9827-9fa060db7338

Public Version Date

July 29, 2020

Public Version Number

1

DI Record Publish Date

July 21, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-