Koalaty Products, Inc. is one of 21470 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Koalaty Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TENS STIMULATOR, MODELS 2800 AND 3000, MODELS TENS 7000, EMS 7500 AND TWIN STIM, MODELS EMS 5.0, EMS 5.1
3
Total
3
Cleared
0
Denied
Koalaty Products, Inc. has 3 FDA 510(k) cleared medical devices. Based in Tampa, US.
Historical record: 3 cleared submissions from 2007 to 2010. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Koalaty Products, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Technology Services, LLC and Underwriters Laboratories, Inc..
FDA 510(k) Regulatory Record - Koalaty Products, Inc.
3 devices