FDA 510(k) K211321 - CProbe Wireless Probe
US FDA 510(k) K211321 for the CProbe wireless probe scanner (types C/L/CT/CL), filed by a SonoStar affiliate. A 510(k) is not FDA approval.
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US FDA 510(k) K211321 for the CProbe wireless probe scanner (types C/L/CT/CL), filed by a SonoStar affiliate. A 510(k) is not FDA approval.