510(k) K792601
K792601 is an FDA 510(k) premarket notification submitted by Corda Int'L Holiday, Inc. for the device "LIFELIFT MODELS ONE AND TWO". The FDA issued a decision of Substantially Equivalent on December 31, 1979. The device falls under product code FSA (Lift, Patient, Non-Ac-Powered), a Class I device regulated under 21 CFR 880.5510.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 31, 1979
- Date Received
- December 18, 1979
- 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