Carticept Medical, Inc.
Carticept Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2015.
Top product codes for Carticept Medical, Inc.
Recent clearances by Carticept Medical, Inc.
- K151255 — Navigator Aesthetic Delivery System
- K124053 — NAVIGATOR DELIVERY SYSTEM (NAVIGATOR DS)
- K122215 — NAVIGATOR DELIVERY SYSTEM (NAVIGATOR DS)
- K120830 — NAVIGATOR DELIVERY SYSTEM (NAVIGATOR DS)
- K112067 — NAVIGATOR DELIVERY SYSTEM (NAVIGATOR DS)
- K101194 — NAVIGATOR DELIVERY SYSTEM (OR NAVIGATOR DS) MODEL: NAV-010
Data sourced from openFDA. This site is unofficial and independent of the FDA.