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 |