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FDA 510(k), K820183, SYBRON/KERR MIRROR 3
FDA 510(k), K820183, SYBRON/KERR MIRROR 3
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510(K) Number: K820183
Device Name: SYBRON/KERR MIRROR 3
Manufacturer:
Device Classification Name: Material, Impression
Regulation Number: ELW
Classification Product Code: 01/22/1982
Date Received: 02/24/1982
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
Device Name: SYBRON/KERR MIRROR 3
Manufacturer:
Device Classification Name: Material, Impression
Regulation Number: ELW
Classification Product Code: 01/22/1982
Date Received: 02/24/1982
Decision Date: Substantially Equivalent (SESE)
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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