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 |