Cooltouch Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cooltouch Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Cooltouch Corp. has 4 FDA 510(k) cleared medical devices. Based in Roseville, US.
Historical record: 4 cleared submissions from 2000 to 2002. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Cooltouch Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cooltouch Corp.
4 devices
Cleared
Mar 07, 2002
COOLTOUCH AND COOLTOUCH-II ND:YAG LASER SYSTEMS
General & Plastic Surgery
90d
Cleared
May 01, 2001
COOLTOUCH VARIA ND:YAG LASER SYSTEM
General & Plastic Surgery
88d
Cleared
Mar 01, 2001
COOLTOUCH ND:YAG LASER SYSTEM, COOLTOUCH-II ND:YAG LASER SYSTEM, MODEL...
General & Plastic Surgery
90d
Cleared
Dec 20, 2000
COOLTOUCH VARIA-II ND:YAG LASER SYSTEM
General & Plastic Surgery
13d