Last synced on 24 May 2024 at 11:04 pm

wheezo WheezeRate Detector

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202062
510(k) Type
Traditional
Applicant
Respiri Limited
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
3/11/2021
Days to Decision
227 days
Submission Type
Summary

wheezo WheezeRate Detector

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202062
510(k) Type
Traditional
Applicant
Respiri Limited
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
3/11/2021
Days to Decision
227 days
Submission Type
Summary