The following data is part of a premarket notification filed by Senticare, Inc. with the FDA for Senticare Pillstation.
| Device ID | K103009 |
| 510k Number | K103009 |
| Device Name: | SENTICARE PILLSTATION |
| Classification | Reminder, Medication |
| Applicant | SENTICARE, INC. 401 9TH STREET NW SUITE 900 Washington, DC 20004 |
| Contact | Seth A Mailhot |
| Correspondent | Seth A Mailhot SENTICARE, INC. 401 9TH STREET NW SUITE 900 Washington, DC 20004 |
| Product Code | NXQ |
| CFR Regulation Number | 890.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-10-12 |
| Decision Date | 2011-01-28 |
| Summary: | summary |