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CELLVIZIO 100 SERIES SYSTEM WITH CONFOCAL MINIPROBES (TM)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133466
510(k) Type
Traditional
Applicant
Mauna Kea Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2014
Days to Decision
255 days
Submission Type
Summary

CELLVIZIO 100 SERIES SYSTEM WITH CONFOCAL MINIPROBES (TM)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133466
510(k) Type
Traditional
Applicant
Mauna Kea Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2014
Days to Decision
255 days
Submission Type
Summary