Catalog Number

2200IC

Brand Name

Bio-Med Devices, Inc.

Version/Model Number

CROSSVENT

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

K942938

Product Code

CBK

Product Code Name

Ventilator, Continuous, Facility Use

Public Device Record Key

7787e945-3878-40fc-8d91-da58a507f998

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

November 02, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-