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510(k) K940872

PATIENT SUPPORT SYSTEM by Arylift, Inc. — Product Code FNG

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 13, 1994
Date Received
February 25, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Lift, Patient, Ac-Powered
Device Class
Class II
Regulation Number
880.5500
Review Panel
HO
Submission Type

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