The following data is part of a premarket notification filed by Core-vent Corp. with the FDA for Micro-vent.
| Device ID | K864321 |
| 510k Number | K864321 |
| Device Name: | MICRO-VENT |
| Classification | Implant, Endosseous, Root-form |
| Applicant | CORE-VENT CORP. 15821 VENTURA BLVD. Encino, CA 91436 |
| Contact | Gerald A Niznick |
| Correspondent | Gerald A Niznick CORE-VENT CORP. 15821 VENTURA BLVD. Encino, CA 91436 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-11-03 |
| Decision Date | 1987-01-07 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MICRO-VENT 73660159 1570757 Dead/Cancelled |
CORE-VENT CORPORATION 1987-05-11 |
![]() MICRO-VENT 73622154 1467275 Dead/Cancelled |
PACKAGING CONCEPTS, INC. 1986-09-25 |
![]() MICRO-VENT 72097192 0710654 Live/Registered |
FELLOWCRAFT ENGINEERING, INC. 1960-05-16 |