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#
- 9611326
- 3005202231
- 3043648106
- 2530138
- 3009407891
- 2529846
- 3016451675
- 3030539818
- 3016661700
- 3005748481
- 3010388769
- 2921578
- 3020460367
- 3010452421
- 3011245426
- 3004133257
- 3001644167
- 1824206
- 1219214
- 9613910
- 3006535976
- 3009008046
- 3026938265
- 3031595580
- 3034520
- 3007802293
- 3008311431
- 3011719799
- 3030432749
- 3007420694
- 3014680784
- 8043351
- 3027782967
- 2090040
- 3017869684
- 2531468
- 3020163307
- 1223962
- 3016746538
- 3040277471
- 3007479130
- 3002786441
- 3010359088
- 3013528589
- 3007710677
- 3005588647
- 3011621895
- 8022890
- 3013410562
- 3005024024
- 3009955851
- 3015443160
- 3019798849
- 1832066
- 3018115441
- 3011647337
- 3030927791
- 3004499949
- 1043214
- 3026523692
- 3014200467
- 3007886583
- 1221921
- 3017085595
- 3010030809
- 1419181
- 3003485057
- 1043644
- 3002637602
- 9710603
- 3010398927
- 1218386
- 3017181414
- 8021894
- 3007441619
- 3005772723
- 3023859
- 3018117722
- 3012330365
Source Documents#
510(k) summary PDF not indicated by FDA