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FDA 510(k), K083811, W&H HANDPIECE ANESTO, MODEL: RA-5
FDA 510(k), K083811, W&H HANDPIECE ANESTO, MODEL: RA-5
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$149.00 USD
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510(K) Number: K083811
Device Name: W&H HANDPIECE ANESTO, MODEL: RA-5
Manufacturer: W & H DENTALWERK BUERMOOS GMBH
Device Classification Name: injector, jet, mechanical-powered
Regulation Number: 872.4475
Classification Product Code: EGM
Date Received: 12/22/2008
Decision Date: 01/14/2010
Regulation Medical Specialty: Dental
Device Name: W&H HANDPIECE ANESTO, MODEL: RA-5
Manufacturer: W & H DENTALWERK BUERMOOS GMBH
Device Classification Name: injector, jet, mechanical-powered
Regulation Number: 872.4475
Classification Product Code: EGM
Date Received: 12/22/2008
Decision Date: 01/14/2010
Regulation Medical Specialty: Dental
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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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