FDA 510(k) Applications Submitted by IKOETECH, LLC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K061006 | 04/11/2006 | IKOENGELO | IKOETECH, LLC. |
| K083591 | 12/04/2008 | IKOENGELO, VERSION 2 | IKOETECH, LLC. |
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