Last synced on 19 July 2024 at 11:05 pm

Breathe+

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222018
510(k) Type
Traditional
Applicant
PEEP Medical LLC dba GO2 Devices
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2023
Days to Decision
329 days
Submission Type
Summary

Breathe+

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222018
510(k) Type
Traditional
Applicant
PEEP Medical LLC dba GO2 Devices
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2023
Days to Decision
329 days
Submission Type
Summary