SENTINEL SYSTEMS
Computer, Diagnostic, Pre-programmed, Single-function
QUANTITATIVE MEDICINE, INC.
The following data is part of a premarket notification filed by Quantitative Medicine, Inc. with the FDA for Sentinel Systems.
Pre-market Notification Details
| Device ID | K833395 |
| 510k Number | K833395 |
| Device Name: | SENTINEL SYSTEMS |
| Classification | Computer, Diagnostic, Pre-programmed, Single-function |
| Applicant | QUANTITATIVE MEDICINE, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DXG |
| CFR Regulation Number | 870.1435 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-09-30 |
| Decision Date | 1984-01-10 |
Trademark Results [SENTINEL SYSTEMS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SENTINEL SYSTEMS 86375092 4816213 Live/Registered |
Cambridge Communications & Signal Systems Corp. 2014-08-22 |
SENTINEL SYSTEMS 86375092 4816213 Live/Registered |
Closed Loop Communications, Inc. 2014-08-22 |
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