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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name probe, radiofrequency lesion
510(k) Number K000073
Device Name MERCURY MEDICAL DISPOSABLE RADIOFREQUENCY CANNULA
Applicant
MERCURY MEDICAL
160 SOUTH MAIN ST.
SUITE A
MIDDLETON,  MA  01949
Applicant Contact MATTHEW NEKOROSKI
Correspondent
MERCURY MEDICAL
160 SOUTH MAIN ST.
SUITE A
MIDDLETON,  MA  01949
Correspondent Contact MATTHEW NEKOROSKI
Regulation Number882.4725
Classification Product Code
GXI  
Date Received01/10/2000
Decision Date 03/01/2000
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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