Altus Medical, Inc. is one of 25321 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
Recent clearances: ALTUS MEDICAL OPTIONAL INFRARED HANDPIECE, ALTUS MEDICAL COOLGLIDE LASER SYSTEMS AND ACCESSORIES, ALTUS MEDICAL FAMILY OF COOLGLIDE LASERS, MODELS COOLGLIDE I, COOLGLIDE II, AND FUTURE MODELS
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.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
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