FDA 510(k) Applications Submitted by NEKS TECHNOLOGIES, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K043156 | 11/15/2004 | D-CARIE, MODEL N121-M1 | NEKS TECHNOLOGIES, INC. |
| K063321 | 11/02/2006 | D-CARIE/DETECTAR, MODELS N121, N123, N133, N134, N135 & N138 | NEKS TECHNOLOGIES, INC. |
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