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 |