American Telecare, Inc. · Class II · Cleared Jun 28, 2001
| K-number | K003999 |
| Device name | AVIVA SYSTEM, MODEL SL 2020; AVIVA SLX SYSTEM SYSTEM, MODEL SLX 1010 |
| Applicant | American Telecare, Inc. |
| Product code | MWI |
| Device class | Class II |
| Decision date | Jun 28, 2001 |
| Decision | Substantially Equivalent |
| Regulation | 870.2300 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov