Last synced on 14 June 2024 at 11:05 pm

CELLVIZIO WITH CONFOCAL MINIPROBES, MODEL F-600; COLOFLEX AND GASTROFLEX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061666
510(k) Type
Special
Applicant
MAUNA KEA TECHNOLOGIES
Country
France
FDA Decision
Substantially Equivalent
Decision Date
8/24/2006
Days to Decision
71 days
Submission Type
Summary