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prolaio eVO2peak Module (Version 1.0)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K252204
510(k) Type
Traditional
Applicant
Prolaio, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2025
Days to Decision
155 days
Submission Type
Summary

prolaio eVO2peak Module (Version 1.0)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K252204
510(k) Type
Traditional
Applicant
Prolaio, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/2025
Days to Decision
155 days
Submission Type
Summary