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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name rongeur, manual
510(k) Number K933978
Device Name NEDBOND EJECTOR KERRISON RONGEUR
Applicant
REDMOND NEUROTECHNOLOGIES CORP.
250 TELSER RD., UNIT E
LAKE ZURICH,  IL  60047
Applicant Contact JONH A REDMOND
Correspondent
REDMOND NEUROTECHNOLOGIES CORP.
250 TELSER RD., UNIT E
LAKE ZURICH,  IL  60047
Correspondent Contact JONH A REDMOND
Regulation Number882.4840
Classification Product Code
HAE  
Date Received08/16/1993
Decision Date 01/12/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
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