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510(k) K910830

INVALIFT by American Invalift Corp. — Product Code FRZ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 9, 1992
Date Received
February 27, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Patient Transfer, Powered
Device Class
Class II
Regulation Number
880.6775
Review Panel
HO
Submission Type

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  • K840796 — TENDER LIFTING CARE (April 20, 1984)