FDA 510(k) Applications Submitted by CAMNTECH, LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K100266 | 01/29/2010 | ACTIWAVE 1E, ACTIWAVE2E, ACTIWAVE2M, ACTIWAVE4E, ACTIWAVE CARDIO MODEL 08-514, 08-521, 08-536, 08-557, 08-603 | CAMNTECH, LTD |
| K132764 | 09/04/2013 | MOTION WATCH AND PRO-DIARY | CAMNTECH, LTD |
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