510(k) K871475
- Device
- SOLOLIFT - PATIENT TRANSFER STRETCHER
- Applicant
- ADEL MEDICAL LTD.
- 510(k) number
- K871475
- Product code
- FMR
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1987-05-11
- Date received
- 1987-04-14
- Regulation
- 880.6785
- Classification name
- Device, Transfer, Patient, Manual
- Medical specialty
- General Hospital
- Review panel
- General Hospital
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- DAVID R COLE
- Address
- 16700 SE 120th Ave. P.O. Box 542 Clackamas OR US 97015 97015
FDA Registration Numbers#
- 3030226293
- 1037752
- 3019585122
- 3030078769
- 1424774
- 8022590
- 3009567010
- 3012137459
- 3015337373
- 3043648106
- 3001124136
- 3009746061
- 1824206
- 1528759
- 3017181414
- 3008518417
- 3008494300
- 3021374638
- 3002786441
- 3026309274
- 8043351
- 3023859
- 3041276591
- 3013557562
- 3010380518
- 3016661700
- 3008381107
- 1220502
- 3026938265
- 3043654660
- 3009512503
- 3003162820
- 3020163307
- 3035782854
- 3014982520
- 3027782967
- 3014270896
- 3003485057
- 1225263
- 3010452421
- 3006560173
- 3012267116
- 3005831263
- 1932271
- 3013528589
- 3010373530
- 3004496839
- 3010030809
- 3015287620
- 1225473
- 9614609
- 3010388471
- 3006795832
- 9681684
- 2921578
- 3022114827
- 3007334893
- 2431497
- 3003827835
- 3026311463
- 3020460367
- 3008311431
- 3026523692
- 1221921
- 3009407891
- 3011767724
- 3008351005
- 3014680784
- 3009327812
- 3011781238
- 3003674698
- 3004905643
- 3013894805
- 3014872186
- 1057079
- 3015443160
- 3010359088
- 3005748481
- 3012330365
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code FMR #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K801796 | THE COMFORT LIFT | Gettner Enterprises, Inc. | 1980-08-13 |
| K800373 | TENDERLIFT | Competent Design | 1980-03-12 |
| K792318 | SKIL-CARE TURN AND HOLD PAD | Skil-Care Corp. | 1979-12-20 |
| K770499 | PATIENT TURNING AND REPOSITIONING G DEV. | Patient Healthguards Corp. | 1977-04-29 |
Legacy Summary#
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FDA Review#
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