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FDA 510(k), K072683, AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM
FDA 510(k), K072683, AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM
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510(K) Number: K072683
Device Name: AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM
Manufacturer: ERIC HASHEMIAN
Device Classification Name: System, Therapeutic, X-Ray
Regulation Number: JAD
Classification Product Code: KXA
Date Received: 09/21/2007
Decision Date: 02/29/2008
Decision Date: SE - With Limitations (SESU)
Regulation Medical Specialty: Radiology
Device Name: AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM
Manufacturer: ERIC HASHEMIAN
Device Classification Name: System, Therapeutic, X-Ray
Regulation Number: JAD
Classification Product Code: KXA
Date Received: 09/21/2007
Decision Date: 02/29/2008
Decision Date: SE - With Limitations (SESU)
Regulation Medical Specialty: Radiology
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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