MICRO-GUIDE
Catheter, Intravascular, Diagnostic
CATHETER RESEARCH C/O BURDITT, BOWLES & RADZIUS
The following data is part of a premarket notification filed by Catheter Research C/o Burditt, Bowles & Radzius with the FDA for Micro-guide.
Pre-market Notification Details
| Device ID | K870700 |
| 510k Number | K870700 |
| Device Name: | MICRO-GUIDE |
| Classification | Catheter, Intravascular, Diagnostic |
| Applicant | CATHETER RESEARCH C/O BURDITT, BOWLES & RADZIUS 333 WEST WACKER DR. SUITE 1900 Chicago, IL 60606 |
| Contact | Joseph R Radzius |
| Correspondent | Joseph R Radzius CATHETER RESEARCH C/O BURDITT, BOWLES & RADZIUS 333 WEST WACKER DR. SUITE 1900 Chicago, IL 60606 |
| Product Code | DQO |
| CFR Regulation Number | 870.1200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-02-19 |
| Decision Date | 1987-12-03 |
Trademark Results [MICRO-GUIDE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MICRO-GUIDE 86429003 4751876 Live/Registered |
Gyrodata Incorporated 2014-10-20 |
 MICRO-GUIDE 86428995 4899299 Live/Registered |
Gyrodata Incorporated 2014-10-20 |
 MICRO-GUIDE 74670917 not registered Dead/Abandoned |
Gillette Company, The 1995-05-08 |
 MICRO-GUIDE 72202738 0802199 Dead/Expired |
BARBER-GREENE COMPANY 1964-09-28 |
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