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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Transport, Patient, Powered
510(k) Number K884110
Device Name LTDT PATIENT LIFTER
Applicant
Devine Medical Products
11677 Hill Rd.
Marysville,  CA  95901
Applicant Contact GARY SCHAAL
Correspondent
Devine Medical Products
11677 Hill Rd.
Marysville,  CA  95901
Correspondent Contact GARY SCHAAL
Regulation Number890.5150
Classification Product Code
ILK  
Date Received09/29/1988
Decision Date 10/13/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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