The following data is part of a premarket notification filed by Mauna Kea Technologies with the FDA for Cellvizio 100 Series System And Cellvizio System With Confocal Miniprobes.
Device ID | K120208 |
510k Number | K120208 |
Device Name: | CELLVIZIO 100 SERIES SYSTEM AND CELLVIZIO SYSTEM WITH CONFOCAL MINIPROBES |
Classification | Confocal Optical Imaging |
Applicant | MAUNA KEA TECHNOLOGIES 8 SNOWBERRY COURT Orinda, CA 94563 |
Contact | Michael A Daniel |
Correspondent | Michael A Daniel MAUNA KEA TECHNOLOGIES 8 SNOWBERRY COURT Orinda, CA 94563 |
Product Code | OWN |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-01-24 |
Decision Date | 2012-04-20 |