FDA 510(k) Applications Submitted by CLAREBLEND, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K073000 | 10/24/2007 | LUMAPROBE | CLAREBLEND, INC. |
| K073022 | 10/26/2007 | CLAREBLEND LED PROBES MODEL# 7201-415, 7204-631, 7205-830 | CLAREBLEND, INC. |
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