510(k) K840997

BATTERY POWERED PATIENT LIFT by Invacare Corp. — Product Code FSA

K840997 is an FDA 510(k) premarket notification submitted by Invacare Corp. for the device "BATTERY POWERED PATIENT LIFT". The FDA issued a decision of Substantially Equivalent on April 17, 1984. The device falls under product code FSA (Lift, Patient, Non-Ac-Powered), a Class I device regulated under 21 CFR 880.5510. Invacare Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 17, 1984
Date Received
March 8, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Lift, Patient, Non-Ac-Powered
Device Class
Class I
Regulation Number
880.5510
Review Panel
HO
Submission Type