FDA 510(k) Applications Submitted by The Binding Site Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K051299 | 05/18/2005 | IGD DIAGNOSTIC TEST KITS | THE BINDING SITE LTD. |
| K231290 | 05/04/2023 | Optilite« Freelite« Kappa Free Kit, Optilite« Freelite« Lambda Free Kit | The Binding Site Ltd. |
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