510(k) K896275
- Device
- JEDMED J-II CHAIR
- Applicant
- JEDMED INSTRUMENT CO.
- 510(k) number
- K896275
- Product code
- FRK
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1989-12-18
- Date received
- 1989-10-30
- 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#
- Contact
- CRAIG RAPP
- Address
- 1430 Hanley Industrial Ct. St. Louis MO US 63144 63144
FDA Registration Numbers#
- 3014471045
- 3008887731
- 1412854
- 3006210673
- 3038718579
- 3001401122
- 3008457024
- 3005688007
- 3015276580
- 3023443842
- 3008346537
- 3043648115
- 3003851947
- 3009408502
- 1625854
- 1000179416
- 3010595915
- 3015168527
- 9681829
- 9616872
- 9710585
- 2951225
- 3015286905
- 3017498782
- 3027847726
- 3017910185
- 1836161
- 1043615
- 3014683120
- 3033433849
- 3026366229
- 3000231798
- 3042989733
- 1063324
- 3010580775
- 3008881803
- 3014273520
- 3025414363
- 3002819275
- 3009817224
- 3000122531
- 1926681
- 3001644167
- 3004905643
- 2182536
- 3007060769
- 1831750
- 3024787345
- 3003524740
- 3014293077
- 1523530
- 3017609565
- 8030607
- 3007912863
- 3003304980
- 3002821232
- 3042255028
- 3010675798
- 3010198795
- 2518399
- 3023859
- 1724810
- 3013408788
- 3008457027
- 3008887767
- 3027320022
- 1062917
- 3013831261
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code FRK #
Legacy Summary#
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FDA Review#
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