Last synced on 21 February 2025 at 11:05 pm

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

Page Type
Product Code
Definition
An infant pulse rate and oxygen saturation monitor for over-the-counter use is a device that uses photoplethysmography to measure pulse rate and oxygen saturation in infants. The device may contain alarms that alert the caregiver when vital sign(s) go outside preset threshold(s).
Physical State
The device worn on the user's foot communicates with a mobile application to display the vital signs for review. Notifications are provided to the caregiver if the device contains alarms.
Technical Method
The device uses photoplethysmography to measure pulse rate and oxygen saturation.
Target Area
The device is worn on the infant's foot.
Regulation Medical Specialty
Cardiovascular
Review Panel
Cardiovascular
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
870.2705
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QYU is linked to regulation 21CFR870.2705, which does not seem to exist yet. It may be pending at the moment.

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

Page Type
Product Code
Definition
An infant pulse rate and oxygen saturation monitor for over-the-counter use is a device that uses photoplethysmography to measure pulse rate and oxygen saturation in infants. The device may contain alarms that alert the caregiver when vital sign(s) go outside preset threshold(s).
Physical State
The device worn on the user's foot communicates with a mobile application to display the vital signs for review. Notifications are provided to the caregiver if the device contains alarms.
Technical Method
The device uses photoplethysmography to measure pulse rate and oxygen saturation.
Target Area
The device is worn on the infant's foot.
Regulation Medical Specialty
Cardiovascular
Review Panel
Cardiovascular
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
870.2705
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QYU is linked to regulation 21CFR870.2705, which does not seem to exist yet. It may be pending at the moment.