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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name anesthesia conduction kit
510(k) Number K925014
Device Name E-SP COMBINED EPI SPINAL MINISET
Applicant
NEURO TECHNOLOGY
P.O. BOX 272123
HOUSTON,  TX  77277
Applicant Contact COOMBS
Correspondent
NEURO TECHNOLOGY
P.O. BOX 272123
HOUSTON,  TX  77277
Correspondent Contact COOMBS
Regulation Number868.5140
Classification Product Code
CAZ  
Date Received10/02/1992
Decision Date 04/19/1993
Decision Substantially Equivalent - Kit (SESK)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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