FDA 510(k), K940120, ALPHA-DENT

FDA 510(k), K940120, ALPHA-DENT

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510(K) Number: K940120
Device Name: ALPHA-DENT
Manufacturer: WALLACE A. ERICKSON & CO.
Device Classification Name: material, impression
Regulation Number: 872.3660
Classification Product Code: ELW
Date Received: 01/10/1994
Decision Date: 02/25/1994
Regulation Medical Specialty: Dental
  • 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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