The following data is part of a premarket notification filed by Chief Medical Llc with the FDA for Carevent.
| Device ID | K062240 |
| 510k Number | K062240 |
| Device Name: | CAREVENT |
| Classification | Accessories, Catheter, G-u |
| Applicant | CHIEF MEDICAL LLC PO BOX 772 105 PIONEER LANE Teton Village, WY 83025 |
| Contact | Scott Horn |
| Correspondent | Scott Horn CHIEF MEDICAL LLC PO BOX 772 105 PIONEER LANE Teton Village, WY 83025 |
| Product Code | KNY |
| CFR Regulation Number | 876.5130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-08-02 |
| Decision Date | 2006-10-16 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CAREVENT 79049368 not registered Dead/Abandoned |
medithek GmbH 2008-01-11 |
![]() CAREVENT 75718937 2640072 Dead/Expired |
O-TWO MEDICAL TECHNOLOGIES INC. 1999-06-03 |