Company ยท US
American Telecare, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 2003. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 19, 2003 | K030222 | NX SYSTEM American Telecare, Inc. | DRG |
| Jun 28, 2001 | K003999 | AVIVA SYSTEM, MODEL SL 2020; AVIVA SLX SYSTEM SYSTEM, MODEL SLX 1010 American Telecare, Inc. | MWI |
| Jan 13, 2000 | K993550 | AVIVA SYSTEM, MODEL SL1010 American Telecare, Inc. | DRG |
| Jul 15, 1998 | K981533 | AVIVA SYSTEMS MODEL NUMBERS 1010, 2020 American Telecare, Inc. | DRG |
| Dec 29, 1997 | K973873 | DIGITAL PERSONAL TELEMEDICINE MODULE, DIGITAL PTM 1 American Telecare, Inc. | DRG |
| Feb 24, 1997 | K963678 | CARETONE II American Telecare, Inc. | DQD |
| Dec 17, 1996 | K964554 | PERSONAL TELEMEDICINE MODULE American Telecare, Inc. | DRG |
| Sep 9, 1996 | K952882 | PERSONAL TELEMEDICINE SYSTEM American Telecare, Inc. | DXN |
| May 17, 1995 | K945638 | TELPHONIC STETHOSCOPE American Telecare, Inc. | DQD |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||