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FDA 510(k), K925080, TEK-LUBE
FDA 510(k), K925080, TEK-LUBE
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$89.00 USD
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510(K) Number: K925080
Device Name: TEK-LUBE
Manufacturer: CLINICAL TECHNOLOGY CORP.
Device Classification Name: Handpiece, Air-Powered, Dental
Regulation Number: 872.4200
Classification Product Code: EFB
Date Received: 10/07/1992
Decision Date: 01/31/1994
Regulation Medical Specialty: Dental
Device Name: TEK-LUBE
Manufacturer: CLINICAL TECHNOLOGY CORP.
Device Classification Name: Handpiece, Air-Powered, Dental
Regulation Number: 872.4200
Classification Product Code: EFB
Date Received: 10/07/1992
Decision Date: 01/31/1994
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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