o_two CPAP - The O-Two single-use open CPAP delivery system - O-Two Medical Technologies Inc

Duns Number:206449154

Device Description: The O-Two single-use open CPAP delivery system provides 5-20 cmH2O CPAP pressure to patie The O-Two single-use open CPAP delivery system provides 5-20 cmH2O CPAP pressure to patients. The adjustment of the CPAP level is achieved by adjusting the output flow from oxygen therapy regulator or wall outlet. The setting selections noted on the device provide an accurate constant airway pressure at each flow setting

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

01CV0211-CS

Brand Name

o_two CPAP

Version/Model Number

01CV0211

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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"

-

For Single-Use

Yes

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

K112546,K112546

Product Code Details

Product Code

BYE

Product Code Name

Attachment, Breathing, Positive End Expiratory Pressure

Device Record Status

Public Device Record Key

bb94fb60-299e-4254-9655-545859a53fc7

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

October 24, 2015

Additional Identifiers

Package DI Number

17540195035031

Quantity per Package

10

Contains DI Package

07540195035034

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton

"O-TWO MEDICAL TECHNOLOGIES INC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 32
2 A medical device with a moderate to high risk that requires special controls. 48
U Unclassified 3