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FDA 510(k), K873604, E.W.L. P-TENS/H-WAVE FOR GENERAL DENTISTRY
FDA 510(k), K873604, E.W.L. P-TENS/H-WAVE FOR GENERAL DENTISTRY
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510(K) Number: K873604
Device Name: E.W.L. P-TENS/H-WAVE FOR GENERAL DENTISTRY
Manufacturer: ELECTRONIC WAVEFORM LABORATORY, INC.
Device Classification Name: device, electrical dental anesthesia
Regulation Number:
Classification Product Code: LWM
Date Received: 09/04/1987
Decision Date: 04/12/1988
Regulation Medical Specialty:
Device Name: E.W.L. P-TENS/H-WAVE FOR GENERAL DENTISTRY
Manufacturer: ELECTRONIC WAVEFORM LABORATORY, INC.
Device Classification Name: device, electrical dental anesthesia
Regulation Number:
Classification Product Code: LWM
Date Received: 09/04/1987
Decision Date: 04/12/1988
Regulation Medical Specialty:
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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