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Revitalair 430+

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220290
510(k) Type
Traditional
Applicant
US Hyperbaric Network
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2023
Days to Decision
457 days
Submission Type
Summary

Revitalair 430+

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220290
510(k) Type
Traditional
Applicant
US Hyperbaric Network
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2023
Days to Decision
457 days
Submission Type
Summary