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Ultra RapidWarm™ Blast

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240605
510(k) Type
Traditional
Applicant
Vitrolife Sweden AB
Country
Sweden
FDA Decision
Substantially Equivalent
Decision Date
8/7/2024
Days to Decision
156 days
Submission Type
Summary

Ultra RapidWarm™ Blast

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240605
510(k) Type
Traditional
Applicant
Vitrolife Sweden AB
Country
Sweden
FDA Decision
Substantially Equivalent
Decision Date
8/7/2024
Days to Decision
156 days
Submission Type
Summary