PRO-GUIDE
Catheter, Percutaneous
AMERICAN INTERVENTIONAL TECHNOLOGY
The following data is part of a premarket notification filed by American Interventional Technology with the FDA for Pro-guide.
Pre-market Notification Details
| Device ID | K911747 |
| 510k Number | K911747 |
| Device Name: | PRO-GUIDE |
| Classification | Catheter, Percutaneous |
| Applicant | AMERICAN INTERVENTIONAL TECHNOLOGY 5157 PARKVIEW CT. Lilburn, GA 30247 |
| Contact | Joe E.brown |
| Correspondent | Joe E.brown AMERICAN INTERVENTIONAL TECHNOLOGY 5157 PARKVIEW CT. Lilburn, GA 30247 |
| Product Code | DQY |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-04-18 |
| Decision Date | 1991-09-18 |
Trademark Results [PRO-GUIDE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PRO-GUIDE 98884650 not registered Live/Pending |
Nu Tsai Capital, LLC 2024-12-04 |
 PRO-GUIDE 88064445 5909551 Live/Registered |
Alum-A-Pole Corporation 2018-08-03 |
 PRO-GUIDE 78107051 2736666 Dead/Cancelled |
HURD, DONALD, J. 2002-02-05 |
 PRO-GUIDE 74334135 1796293 Live/Registered |
BATTERY OUTFITTERS, INC. 1992-11-24 |
 PRO-GUIDE 73474255 1345625 Dead/Cancelled |
WATER BUSTER, INC. 1984-04-09 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.