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#
- 3029923680
- 3006795832
- 3009327812
- 3002637602
- 3008381107
- 3004499949
- 3016746538
- 3009600453
- 3002786441
- 3025355675
- 3008918830
- 3030233125
- 2183887
- 3007420694
- 2182762
- 2531468
- 1060680
- 1220502
- 3032391
- 3005034064
- 3036731074
- 3011495193
- 3042871597
- 3010030809
- 8010730
- 3010373263
- 9611326
- 3038623066
- 3003162820
- 3007334893
- 3014270896
- 3013894805
- 3011719799
- 3023852281
- 3007479130
- 3015007646
- 3030927791
- 3012137459
- 1931307
- 3001124136
- 3007886583
- 3010373530
- 3020163307
- 1223962
- 3014200467
- 1221921
- 3005755627
- 3014680784
- 1027229
- 9613910
- 3024761165
- 3015423385
- 3012643605
- 3013528589
- 3014982520
- 3026818268
- 3015068387
- 3019991551
- 3003485057
- 3008603863
- 1225263
- 3023194188
- 3010398927
- 3017869684
- 3017085595
- 3026309274
- 1225473
- 3007309299
- 3005024024
- 3009350690
- 3006560173
- 3019585122
- 1043572
- 9680168
- 1836161
- 3006802326
- 3018117722
- 3016661700
- 3020282968
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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