FDA 510(k), K925080, TEK-LUBE

FDA 510(k), K925080, TEK-LUBE

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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

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