THE COMFORT LIFT
FDA 510(k) clearance K801796 · decided 1980-08-13
Clearance details
- K-number
- K801796
- Device name
- THE COMFORT LIFT
- Applicant
- Gettner Enterprises, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1980-07-29
- Decision date
- 1980-08-13
- Days to decision
- 15 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 |
| TENDERLIFT (K800373) | Competent Design | 1980-03-12 |
| 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.