MINI-PORT
Catheter, Peritoneal
TAUT, INC.
The following data is part of a premarket notification filed by Taut, Inc. with the FDA for Mini-port.
Pre-market Notification Details
| Device ID | K992904 |
| 510k Number | K992904 |
| Device Name: | MINI-PORT |
| Classification | Catheter, Peritoneal |
| Applicant | TAUT, INC. 2571 KANEVILLE COURT Geneva, IL 60134 |
| Contact | Ronald Kenseth |
| Correspondent | Ronald Kenseth TAUT, INC. 2571 KANEVILLE COURT Geneva, IL 60134 |
| Product Code | GBW |
| CFR Regulation Number | 878.4200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-08-30 |
| Decision Date | 1999-10-05 |
Trademark Results [MINI-PORT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MINI-PORT 78139445 2728444 Dead/Cancelled |
Byrne Electrical Specialists, Inc. 2002-06-27 |
 MINI-PORT 77756467 3823840 Live/Registered |
Byrne Electrical Specialists, Inc. 2009-06-10 |
 MINI-PORT 74246072 not registered Dead/Abandoned |
Woodhead Industries, Inc. 1992-02-13 |
 MINI-PORT 73547977 1380441 Dead/Cancelled |
HAZEL, INC. 1985-07-15 |
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