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FDA 510(k), K091106, EQUIA
FDA 510(k), K091106, EQUIA
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510(K) Number: K091106
Device Name: EQUIA
Manufacturer: GC AMERICA, INC.
Device Classification Name: cement, dental
Regulation Number: 872.3275
Classification Product Code: EMA
Date Received: 04/16/2009
Decision Date: 06/17/2009
Regulation Medical Specialty: Dental
Device Name: EQUIA
Manufacturer: GC AMERICA, INC.
Device Classification Name: cement, dental
Regulation Number: 872.3275
Classification Product Code: EMA
Date Received: 04/16/2009
Decision Date: 06/17/2009
Regulation Medical Specialty: Dental
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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