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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
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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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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