Q3000
Computer, Diagnostic, Programmable
QUINTON, INC.
The following data is part of a premarket notification filed by Quinton, Inc. with the FDA for Q3000.
Pre-market Notification Details
| Device ID | K834567 |
| 510k Number | K834567 |
| Device Name: | Q3000 |
| Classification | Computer, Diagnostic, Programmable |
| Applicant | QUINTON, INC. WA |
| Product Code | DQK |
| CFR Regulation Number | 870.1425 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-12-28 |
| Decision Date | 1984-04-30 |
Trademark Results [Q3000]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 Q3000 75793324 2577086 Dead/Cancelled |
Advanced Motion Technologies 1999-09-07 |
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