Last synced on 19 July 2024 at 11:05 pm

CELLVIZIO 100 SERIES SYSTEM AND CELLVIZIO SYSTEM WITH CONFOCAL MINIPROBES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120208
510(k) Type
Special
Applicant
MAUNA KEA TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/2012
Days to Decision
87 days
Submission Type
Summary

CELLVIZIO 100 SERIES SYSTEM AND CELLVIZIO SYSTEM WITH CONFOCAL MINIPROBES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120208
510(k) Type
Special
Applicant
MAUNA KEA TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/20/2012
Days to Decision
87 days
Submission Type
Summary