FDA 510(k), K791013, SPECTRA R PAD

FDA 510(k), K791013, SPECTRA R PAD

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510(K) Number: K791013
Device Name: SPECTRA R PAD
Manufacturer: PARKER LABORATORIES, INC.
Device Classification Name: media, electroconductive
Regulation Number: 882.1275
Classification Product Code: GYB
Date Received: 06/01/1979
Decision Date: 09/17/1979
Regulation Medical Specialty: Neurology

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