The following data is part of a premarket notification filed by Pascal Co., Inc. with the FDA for Occlude.
| Device ID | K912632 |
| 510k Number | K912632 |
| Device Name: | OCCLUDE |
| Classification | Paper, Articulation |
| Applicant | PASCAL CO., INC. P.O. BOX 1478 Bellevue, WA 98009 |
| Contact | Joe Pellicano |
| Correspondent | Joe Pellicano PASCAL CO., INC. P.O. BOX 1478 Bellevue, WA 98009 |
| Product Code | EFH |
| CFR Regulation Number | 872.6140 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-06-14 |
| Decision Date | 1992-01-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() OCCLUDE 77478347 not registered Dead/Abandoned |
EndoShape, Inc. 2008-05-19 |
![]() OCCLUDE 75600777 2304233 Dead/Cancelled |
INTERNATIONAL FLOW TECHNOLOGIES, INC. 1998-12-07 |
![]() OCCLUDE 73015843 1012777 Live/Registered |
PASCAL COMPANY, INC. 1974-03-13 |