A.C. Power Patient Lift
FDA 510(k) K935351 · Ken Kemmerer
510(k) numberK935351
Submission
- Device name
- A.C. Power Patient Lift
- Applicant
- Ken Kemmerer
Wilkes Barre Twp, PA, US - Received
- November 5, 1993
- Decision date
- February 28, 1994
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- FNG – Lift, Patient, Ac-Powered
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5500
- Specialty
- General Hospital
Other 510(k)s with product code FNG
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K121287 | Ht-WedgeFNG · Traditional | D.T. Davis Enterprises Ltd. T/A Hovertech Int'L | 10/03/2012SE |
| K041503 | Hoverjack Air Patient Lift DeviceFNG · Traditional | D.T. Davis Enterprises , Ltd. | 08/12/2004SE |
| K940872 | Patient Support SystemFNG · Traditional | Arylift, Inc. | 10/13/1994SE |
| K926411 | Saf-Lift/Saf-KaryFNG · Traditional | Arjo-Century, Inc. | 03/31/1993SE |
| K912769 | Patient Lift and TransportFNG · Traditional | Century Manufacturing Co. | 10/02/1991SE |
| K905414 | Mangar BoosterFNG · Traditional | Northfleet Management Group, Inc. | 03/05/1991SE |
| K895677 | The Murray Mobilift(Tm)FNG · Traditional | Medical/Surgical Specialties, Ltd. | 10/26/1990SE |
| K903723 | Barrier Free Ceiling Lift, MDLS HRS-1/2F,1/4F,1/6FFNG · Traditional | Barrier Free Lifts, Inc. | 09/24/1990SE |
| K896848 | Lift Master Patient LiftFNG · Traditional | Henry Enterprises, Inc. | 05/29/1990SE |
| K885270 | Personal Transfer SystemFNG · Traditional | Columbus Mckinnon Corp. | 03/14/1989SE |
More from Columbus Mckinnon Corp.
| 510(k) | Device | Decision |
|---|---|---|
| K961663 | Electric Seat Lift ChairINO · Traditional | 05/29/1996SE |
Questions and answers
When was A.C. Power Patient Lift cleared by the FDA?
A.C. Power Patient Lift (K935351) received a 510(k) decision of Substantially Equivalent on February 28, 1994, 115 days after the submission was received.
What is the product code of K935351?
The FDA product code is FNG – Lift, Patient, Ac-Powered, a Class II (moderate risk) device regulated under 21 CFR 880.5500.