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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 K904261
Device Name LITTER, NONRIDGID, POLELESS, NYLON STRETCHER
Applicant
Dow Cover Co., Inc.
373 Lexington Ave.
New Haven,  CT  06513
Applicant Contact MARK STEINHARDT
Correspondent
Dow Cover Co., Inc.
373 Lexington Ave.
New Haven,  CT  06513
Correspondent Contact MARK STEINHARDT
Regulation Number880.6900
Classification Product Code
FPP  
Date Received09/14/1990
Decision Date 10/12/1990
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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