The following data is part of a premarket notification filed by Vocel with the FDA for Pill Phone.
| Device ID | K060298 |
| 510k Number | K060298 |
| Device Name: | PILL PHONE |
| Classification | Reminder, Medication |
| Applicant | VOCEL 1425 K STREET, N.W. SUITE 1100 Washington, DC 20005 |
| Contact | Keith A Barritt |
| Correspondent | Keith A Barritt VOCEL 1425 K STREET, N.W. SUITE 1100 Washington, DC 20005 |
| Product Code | NXQ |
| CFR Regulation Number | 890.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-02-06 |
| Decision Date | 2006-03-29 |
| Summary: | summary |