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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stretcher, Wheeled
510(k) Number K863083
Device Name BETA MEDICAL PRODUCTS EMR-301 HYDRAULIC STRETCHER
Applicant
Beta Medical Products Co.
Suite A7, 46 Ravenna St.
Hudson,  OH  44236
Applicant Contact KEVIN BENOIT
Correspondent
Beta Medical Products Co.
Suite A7, 46 Ravenna St.
Hudson,  OH  44236
Correspondent Contact KEVIN BENOIT
Regulation Number880.6910
Classification Product Code
FPO  
Date Received08/12/1986
Decision Date 09/03/1986
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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