Altus Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Altus Medical, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Altus Medical, Inc. has 4 FDA 510(k) cleared medical devices. Based in Burlingame, US.
Historical record: 4 cleared submissions from 2002 to 2004. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Altus Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Altus Medical, Inc.
4 devices
Cleared
Feb 17, 2004
ALTUS MEDICAL OPTIONAL INFRARED HANDPIECE
Physical Medicine
76d
Cleared
Mar 18, 2003
ALTUS MEDICAL COOLGLIDE LASER SYSTEMS AND ACCESSORIES
General & Plastic Surgery
111d
Cleared
Oct 08, 2002
ALTUS MEDICAL FAMILY OF COOLGLIDE LASERS, MODELS COOLGLIDE I, COOLGLIDE II,...
General & Plastic Surgery
90d
Cleared
Jun 03, 2002
FAMILY OF ALTUS MEDICAL MODIFIED COOLGLIDE AESTHETIC LASERS, MODELS COOLGLIDE...
General & Plastic Surgery
178d