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FDA 510(k), K120372, DR GREENBURGS HYBRID VACUUM
FDA 510(k), K120372, DR GREENBURGS HYBRID VACUUM
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$149.00 USD
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510(K) Number: K120372
Device Name: DR GREENBURGS HYBRID VACUUM
Manufacturer: ALWAYS MORE MARKETING INC
Device Classification Name: device, anti-snoring
Regulation Number: 872.5570
Classification Product Code: LRK
Date Received: 02/06/2012
Decision Date: 06/27/2012
Regulation Medical Specialty: Dental
Device Name: DR GREENBURGS HYBRID VACUUM
Manufacturer: ALWAYS MORE MARKETING INC
Device Classification Name: device, anti-snoring
Regulation Number: 872.5570
Classification Product Code: LRK
Date Received: 02/06/2012
Decision Date: 06/27/2012
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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