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SERENITY PRO PSF SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071943
510(k) Type
Special
Applicant
Inolase 2002, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/2007
Days to Decision
28 days
Submission Type
Summary

SERENITY PRO PSF SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071943
510(k) Type
Special
Applicant
Inolase 2002, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/2007
Days to Decision
28 days
Submission Type
Summary