Tender Lifting Care
FDA 510(k) K840796 · Lancer Assoc.
510(k) numberK840796
Submission
- Device name
- Tender Lifting Care
- Applicant
- Lancer Assoc.
Walker, MI, US - Received
- February 23, 1984
- Decision date
- April 20, 1984
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- FRZ – Device, Patient Transfer, Powered
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.6775
- Specialty
- General Hospital
Other 510(k)s with product code FRZ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K121929 | Zephyr 'X-Series Patient Transfer SledFRZ · Traditional | Diacor, Inc. | 01/17/2013SE |
| K910830 | InvaliftFRZ · Traditional | American Invalift Corp. | 06/09/1992SE |
| K841728 | Lci Medical Inc Air/PalFRZ · Traditional | Lehigh Consolidated Industries | 06/05/1984SE |
| K834585 | Celltrak-BFRZ · Traditional | R&D Systems, Inc. | 05/02/1984SE |
More from R&D Systems, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K831033 | GirexION · Traditional | 04/27/1983SE |
Questions and answers
When was Tender Lifting Care cleared by the FDA?
Tender Lifting Care (K840796) received a 510(k) decision of Substantially Equivalent on April 20, 1984, 57 days after the submission was received.
What is the product code of K840796?
The FDA product code is FRZ – Device, Patient Transfer, Powered, a Class II (moderate risk) device regulated under 21 CFR 880.6775.