Catalog Number

-

Brand Name

Respire Pink AT EF

Version/Model Number

SPAT030US

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

K192127

Product Code

LRK

Product Code Name

Device, Anti-Snoring

Public Device Record Key

99fc4af5-1454-4c61-b82b-7b65797d0da1

Public Version Date

February 21, 2020

Public Version Number

1

DI Record Publish Date

February 13, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-