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Humask Pro Vision, Humask Pro Vision 3000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222551
510(k) Type
Abbreviated
Applicant
Entreprise Premont, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
11/10/2022
Days to Decision
79 days
Submission Type
Summary

Humask Pro Vision, Humask Pro Vision 3000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222551
510(k) Type
Abbreviated
Applicant
Entreprise Premont, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
11/10/2022
Days to Decision
79 days
Submission Type
Summary