Last synced on 14 November 2025 at 11:06 pm

RespiraSense

Page Type
Cleared 510(K)
510(k) Number
K220111
510(k) Type
Traditional
Applicant
PMD Solutions
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
10/7/2022
Days to Decision
267 days
Submission Type
Summary

RespiraSense

Page Type
Cleared 510(K)
510(k) Number
K220111
510(k) Type
Traditional
Applicant
PMD Solutions
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
10/7/2022
Days to Decision
267 days
Submission Type
Summary