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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 K943864
Device Name STRYKER 8000 SURGERY STRETCHER
Applicant
STRYKER MEDICAL
6300 S. SPRINKLE RD.
KALAMAZOO,  MI  49001 -9799
Applicant Contact CHAD A COBERLY
Correspondent
STRYKER MEDICAL
6300 S. SPRINKLE RD.
KALAMAZOO,  MI  49001 -9799
Correspondent Contact CHAD A COBERLY
Regulation Number880.6910
Classification Product Code
FPO  
Date Received08/08/1994
Decision Date 08/25/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
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