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FDA 510(k), K111680, DR. GREENSBURG'S HYBRID
FDA 510(k), K111680, DR. GREENSBURG'S HYBRID
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$49.00 USD
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510(K) Number: K111680
Device Name: DR. GREENSBURG'S HYBRID
Manufacturer: ALWAYS MORE MARKETING INC
Device Classification Name: device, anti-snoring
Regulation Number: 872.5570
Classification Product Code: LRK
Date Received: 06/15/2011
Decision Date: 12/23/2011
Regulation Medical Specialty: Dental
Device Name: DR. GREENSBURG'S HYBRID
Manufacturer: ALWAYS MORE MARKETING INC
Device Classification Name: device, anti-snoring
Regulation Number: 872.5570
Classification Product Code: LRK
Date Received: 06/15/2011
Decision Date: 12/23/2011
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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