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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Monitor, Patient Position, Light-Beam
510(k) Number K930294
Device Name PATPOS GREEN
Applicant
Cp Bio-Medical Corp.
153 E.Palmetto Park Rd.
Suite 133
Boca Raton,  FL  33432
Applicant Contact VAN ARKEL
Correspondent
Cp Bio-Medical Corp.
153 E.Palmetto Park Rd.
Suite 133
Boca Raton,  FL  33432
Correspondent Contact VAN ARKEL
Regulation Number892.5780
Classification Product Code
IWE  
Date Received01/21/1993
Decision Date 06/04/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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