Duns Number:059636679
Device Description: Intraoral device for the treatment of snoring and mild to moderate obstructive sleep apnea
Catalog Number
-
Brand Name
Respire Pink EF+
Version/Model Number
SPP030US
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 23, 2018
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
K150572
Product Code
LRK
Product Code Name
Device, Anti-Snoring
Public Device Record Key
ba788f69-3b78-405d-8391-70bd2787f133
Public Version Date
February 17, 2020
Public Version Number
6
DI Record Publish Date
September 15, 2017
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 28 |