510(k) K840997
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