TENDERLIFT
FDA 510(k) clearance K800373 · decided 1980-03-12
Clearance details
- K-number
- K800373
- Device name
- TENDERLIFT
- Applicant
- Competent Design
- Decision
- Substantially Equivalent
- Date received
- 1980-02-20
- Decision date
- 1980-03-12
- Days to decision
- 21 days
- Clearance type
- Traditional
- Product code
- FMR
- Device class
- 1
- Regulation number
- 880.6785
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| SOLOLIFT - PATIENT TRANSFER STRETCHER (K871475) | Adel Medical , Ltd. | 1987-05-11 |
| THE COMFORT LIFT (K801796) | Gettner Enterprises, Inc. | 1980-08-13 |
| SKIL-CARE TURN AND HOLD PAD (K792318) | Skil-Care Corp. | 1979-12-20 |
| PATIENT TURNING AND REPOSITIONING G DEV. (K770499) | Patient Healthguards Corp. | 1977-04-29 |
Recalls involving this device
No recalls on record reference this clearance.