FDA medical devices database
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Scan day: 08 March 2014 UTC
7
Virus safety - good
Description: Type KTH in the product code for a list of all anti-stuttering devices cleared for marketing in the United States.
U.S. Food & Drug Administration Vaccines, Blood & Biologics A 510(K) is a premarket submission made to FDA to demonstrate that the device to be marketed is at least as safe and effective, that is, substantially equivalent, to a legally marketed device (21 CFR §
Size: 278 chars
Contact Information
Email: —
Phone&Fax: 888-463-6332
Address: —
Extended: —
WEBSITE Info
| Page title: | 510(k) Premarket Notification |
| Keywords: | |
| Description: | |
| IP-address: | 95.100.0.141 |
WHOIS Info
| NS | |
| WHOIS | Status: ACTIVE |
| Date |