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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 K920704
Device Name STRYKER I.V. CADDY ACCESSORY DEVICE
Applicant
STRYKER MEDICAL
6300 S. SPRINKLE RD.
KALAMAZOO,  MI  49001 -9799
Applicant Contact JAMES A AHLE
Correspondent
STRYKER MEDICAL
6300 S. SPRINKLE RD.
KALAMAZOO,  MI  49001 -9799
Correspondent Contact JAMES A AHLE
Regulation Number880.6910
Classification Product Code
FPO  
Date Received02/18/1992
Decision Date 03/23/1992
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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