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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 K940130
Device Name STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER
Applicant
Stryker Corp.
Medical Div.
6300 Sprinkle Rd.
Kalamazoo,  MI  49001
Applicant Contact SCOTT GIAMBALVO
Correspondent
Stryker Corp.
Medical Div.
6300 Sprinkle Rd.
Kalamazoo,  MI  49001
Correspondent Contact SCOTT GIAMBALVO
Regulation Number880.6900
Classification Product Code
FPP  
Date Received01/03/1994
Decision Date 03/10/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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