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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
510(k) Number K871546
Device Name SAFESIDE(TM) LUMED
Applicant
Luther Medical Products, Inc.
1940 E. Occidental St.
Santa Ana,  CA  92705
Applicant Contact RONALD B LUTHER
Correspondent
Luther Medical Products, Inc.
1940 E. Occidental St.
Santa Ana,  CA  92705
Correspondent Contact RONALD B LUTHER
Regulation Number880.5200
Classification Product Code
FOZ  
Date Received04/20/1987
Decision Date 06/17/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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