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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name catheter, conduction, anesthetic
510(k) Number K850505
Device Name DESERET EPIDURAL CATHETER W/TOUGHY-BORST ADAPTER
Applicant
PARKE-DAVIS CO.
870 PARKDALE RD.
ROCHESTER,  MI  48307
Applicant Contact CLEARY
Correspondent
PARKE-DAVIS CO.
870 PARKDALE RD.
ROCHESTER,  MI  48307
Correspondent Contact CLEARY
Regulation Number868.5120
Classification Product Code
BSO  
Date Received02/08/1985
Decision Date 03/11/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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