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CRYOPRO MAXI AND CRYOPRO MINI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982280
510(k) Type
Traditional
Applicant
CORTEX TECHNOLOGY APS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/1998
Days to Decision
148 days
Submission Type
Summary

CRYOPRO MAXI AND CRYOPRO MINI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982280
510(k) Type
Traditional
Applicant
CORTEX TECHNOLOGY APS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/1998
Days to Decision
148 days
Submission Type
Summary