510(k) K791016
- Device
- ULTICARE 2500 TREATMENT CHAIR
- Applicant
- American Health Care Industries, Inc.
- 510(k) number
- K791016
- Product code
- FRK
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1979-06-27
- Date received
- 1979-06-01
- Regulation
- 880.6140
- Classification name
- Chair, Examination And Treatment
- Medical specialty
- General Hospital
- Review panel
- General Hospital
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3003851947
- 1063324
- 1926681
- 3033433849
- 1000179416
- 3010198795
- 3010595915
- 3004905643
- 1062917
- 1836161
- 9616872
- 1412854
- 3013408788
- 3010675798
- 1724810
- 3007912863
- 3015276580
- 3009408502
- 3002821232
- 3042255028
- 2518399
- 3001644167
- 3024787345
- 3009817224
- 3008887767
- 2951225
- 3002819275
- 3014293077
- 3003524740
- 3038718579
- 3017609565
- 3042989733
- 3023859
- 3017910185
- 3015168527
- 3008457024
- 3008346537
- 3008457027
- 9681829
- 2182536
- 3014273520
- 3015286905
- 3027320022
- 9710585
- 3027847726
- 3003304980
- 3008887731
- 3014683120
- 3025414363
- 3006210673
- 3013831261
- 1625854
- 3007060769
- 3000122531
- 8030607
- 3023443842
- 3010580775
- 3005688007
- 3001401122
- 3043648115
- 1043615
- 3014471045
- 3017498782
- 3026366229
- 3008881803
- 1523530
- 1831750
- 3000231798
Source Documents#
510(k) summary PDF not indicated by FDA