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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Catheter, Straight
510(k) Number K944383
Device Name ORION RED URETHRAL CATHETER
Applicant
REGULATORY & MARKETING SERVICES, INC.
1247 FLORIDA AVE.
PALM HARBOR,  FL  34682
Applicant Contact PATRICK J LAMB
Correspondent
REGULATORY & MARKETING SERVICES, INC.
1247 FLORIDA AVE.
PALM HARBOR,  FL  34682
Correspondent Contact PATRICK J LAMB
Regulation Number876.5130
Classification Product Code
EZD  
Subsequent Product Code
GBM  
Date Received09/07/1994
Decision Date 12/06/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
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