The following data is part of a premarket notification filed by Travis Industries, Inc. with the FDA for Professional Monitor.
| Device ID | K901907 |
| 510k Number | K901907 |
| Device Name: | PROFESSIONAL MONITOR |
| Classification | Alarm, Conditioned Response Enuresis |
| Applicant | TRAVIS INDUSTRIES, INC. 100 MAIN-SUMNER Coos Bay, OR 97420 |
| Contact | Keith A Brown |
| Correspondent | Keith A Brown TRAVIS INDUSTRIES, INC. 100 MAIN-SUMNER Coos Bay, OR 97420 |
| Product Code | KPN |
| CFR Regulation Number | 876.2040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-04-27 |
| Decision Date | 1990-09-12 |