Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

American Telecare, Inc.

FDA 510(k) & PMA Approved Devices — 9 products

Total Devices9
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K030222 NX SYSTEMDRG2003-08-19 View
510(k) K003999 AVIVA SYSTEM, MODEL SL 2020; AVIVA SLX SYSTEM SYSTEM, MODEL SLX 1010MWI2001-06-28 View
510(k) K993550 AVIVA SYSTEM, MODEL SL1010DRG2000-01-13 View
510(k) K981533 AVIVA SYSTEMS MODEL NUMBERS 1010, 2020DRG1998-07-15 View
510(k) K973873 DIGITAL PERSONAL TELEMEDICINE MODULE, DIGITAL PTM 1DRG1997-12-29 View
510(k) K963678 CARETONE IIDQD1997-02-24 View
510(k) K964554 PERSONAL TELEMEDICINE MODULEDRG1996-12-17 View
510(k) K952882 PERSONAL TELEMEDICINE SYSTEMDXN1996-09-09 View
510(k) K945638 TELPHONIC STETHOSCOPEDQD1995-05-17 View
↑