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FDA 510(k), K925378, STERI-SOL SOLUTION, MODIFICATION
FDA 510(k), K925378, STERI-SOL SOLUTION, MODIFICATION
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510(K) Number: K925378
Device Name: STERI-SOL SOLUTION, MODIFICATION
Manufacturer: THAD J OVERMYER
Device Classification Name: Handpiece, Air-Powered, Dental
Regulation Number: EFB
Classification Product Code: KXA
Date Received: 10/06/1992
Decision Date: 07/22/1993
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
Device Name: STERI-SOL SOLUTION, MODIFICATION
Manufacturer: THAD J OVERMYER
Device Classification Name: Handpiece, Air-Powered, Dental
Regulation Number: EFB
Classification Product Code: KXA
Date Received: 10/06/1992
Decision Date: 07/22/1993
Decision: Substantially Equivalent (SESE)
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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