510(k) K770499
- Device
- PATIENT TURNING AND REPOSITIONING G DEV.
- Applicant
- Patient Healthguards Corp.
- 510(k) number
- K770499
- Product code
- FMR
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-04-29
- Date received
- 1977-03-14
- 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
- N
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
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