FDA 510(k), K122413, PATIENT POSITIONING SYSTEM
FDA 510(k), K122413, PATIENT POSITIONING SYSTEM
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$149.00 USD
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510(K) Number: K122413
Device Name: PATIENT POSITIONING SYSTEM
Manufacturer:
Device Classification Name: Couch, Radiation Therapy, Powered
Regulation Number: 892.5770
Classification Product Code: JAI
Date Received: 08/08/2012
Decision Date: 09/13/2012
Regulation Medical Specialty: Radiology
Device Name: PATIENT POSITIONING SYSTEM
Manufacturer:
Device Classification Name: Couch, Radiation Therapy, Powered
Regulation Number: 892.5770
Classification Product Code: JAI
Date Received: 08/08/2012
Decision Date: 09/13/2012
Regulation Medical Specialty: Radiology