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RAPIDVIT AND RAPIDWARM CLEAVE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080446
510(k) Type
Traditional
Applicant
Vitrolife Sweden AB
Country
Sweden
FDA Decision
Substantially Equivalent
Decision Date
11/26/2008
Days to Decision
281 days
Submission Type
Summary

RAPIDVIT AND RAPIDWARM CLEAVE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080446
510(k) Type
Traditional
Applicant
Vitrolife Sweden AB
Country
Sweden
FDA Decision
Substantially Equivalent
Decision Date
11/26/2008
Days to Decision
281 days
Submission Type
Summary