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FDA 510(k), K014027, OPTIBOND SOLO PLUS 4
FDA 510(k), K014027, OPTIBOND SOLO PLUS 4
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510(K) Number: K014027
Device Name: OPTIBOND SOLO PLUS 4
Manufacturer: KERR DENTAL MATERIALS CENTER
Device Classification Name: agent, tooth bonding, resin
Regulation Number: 872.3200
Classification Product Code: KLE
Date Received: 12/06/2001
Decision Date: 02/22/2002
Regulation Medical Specialty: Dental
Device Name: OPTIBOND SOLO PLUS 4
Manufacturer: KERR DENTAL MATERIALS CENTER
Device Classification Name: agent, tooth bonding, resin
Regulation Number: 872.3200
Classification Product Code: KLE
Date Received: 12/06/2001
Decision Date: 02/22/2002
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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