Catalog Number

-

Brand Name

SomnoGuard AP 2

Version/Model Number

03050200

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

-

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

K061688

Product Code

LRK

Product Code Name

Device, Anti-Snoring

Public Device Record Key

57796cc4-f03c-43a0-821b-3f79435ba71b

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

January 01, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-