FDA 510(k), K033967, TELETHERMOGRAPHIC CAMERA, SERIES A, E, S AND P

FDA 510(k), K033967, TELETHERMOGRAPHIC CAMERA, SERIES A, E, S AND P

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510(K) Number: K033967
Device Name: TELETHERMOGRAPHIC CAMERA, SERIES A, E, S AND P
Manufacturer:
Device Classification Name: System, Telethermographic (Adjunctive Use)
Regulation Number: 884.2980
Classification Product Code: LHQ
Date Received: 12/22/2003
Decision Date: 03/09/2004
Regulation Medical Specialty: Obstetrics/Gynecology
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