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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 K991879
Device Name SPRING-WOUND EPIDURAL CATHETER
Applicant
Micor, Inc.
2855 Oxford Blvd.
Allison Park,  PA  15101
Applicant Contact CHARLES W ESLEEP
Correspondent
Micor, Inc.
2855 Oxford Blvd.
Allison Park,  PA  15101
Correspondent Contact CHARLES W ESLEEP
Regulation Number868.5120
Classification Product Code
BSO  
Date Received06/02/1999
Decision Date 10/28/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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