FDA UDI In Commercial Distribution 🇺🇸 United States

Dream Sock App

DI: 00810099090819 · Model: 3.0 · Owlet Baby Care Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Dream Sock App
Primary DI
00810099090819
Version / Model
3.0
Company Name
Owlet Baby Care Inc.
Labeler DUNS
079422657
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-12
Public Version
1
Public Version Date
2024-02-20
Public Version Status
New
Public Device Record Key
c1f967ea-e056-49b2-a909-2e95ed1e8da9

Device Description

Dream Sock Software App. The Dream Sock is intended for over-the-counter (OTC) use only in a home environment. It is not intended to provide notification for every episode of the unexpected occurrences of elevated or depressed PR or a low SpO2 level; rather, the Dream Sock is intended to provide a notification only when sufficient data are available for analysis. The notifications and associated data can be used to supplement the decision by caregivers to seek additional guidance for medical care of the infant. The Dream Sock is not intended to replace traditional methods of monitoring, diagnosis or treatment.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QYU Infant Pulse Rate And Oxygen Saturation Monitor For Over-The-Counter Use

GMDN Terms

Code Name
65669 Multiple vital physiological parameter monitoring system, home-use

Identifiers

Type ID
Primary 00810099090819

Premarket Submissions

Submission Number Supplement Number
DEN220091 000