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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stretcher, Hand-Carried
510(k) Number K896261
Device Name THE SMITHCOT
Applicant
Ram Marketing, Inc.
1641 Broad St.
Greensburg,  PA  15601
Applicant Contact THOMAS L CROSS
Correspondent
Ram Marketing, Inc.
1641 Broad St.
Greensburg,  PA  15601
Correspondent Contact THOMAS L CROSS
Regulation Number880.6900
Classification Product Code
FPP  
Date Received10/30/1989
Decision Date 12/22/1989
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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