510(k) K894788
- Device
- Dmi Series 90 Examination Table
- Applicant
- M.D. INTL., INC.
- 510(k) number
- K894788
- Product code
- KMN
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1989-09-08
- Date received
- 1989-07-28
- Regulation
- 880.6140
- Classification name
- Chair And Table, Medical
- Medical specialty
- General Hospital
- Review panel
- General Hospital
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- JOHANNE D YOUNG
- Address
- 2601 S. 2700 W. Salt Lake City UT US 84119 84119
FDA Registration Numbers#
- 3005214422
- 3042989733
- 3011574775
- 3009952786
- 3004034546
- 3012709011
- 1926681
- 3005651859
- 3044829820
- 3014982318
- 9681454
- 3006897028
- 3010605276
- 3014498763
- 2242467
- 3007607706
- 3026311463
- 3043460907
- 3017278503
- 3027643666
- 3008881803
- 3010509576
- 3014810929
- 3016162044
- 3030488262
- 3042970964
- 2432177
- 3011621895
- 1836161
- 1000122786
- 3037012186
- 1422443
- 9615415
- 9616086
- 3010411316
- 3012316249
- 3010373530
- 1417592
- 3031082325
- 3016915446
- 3013495708
- 3004186402
- 3039065815
- 1831750
- 3009425497
- 3014471045
- 8030607
- 3009157571
- 3016678414
- 3013903013
- 3027332478
- 3016678950
- 3005545844
- 3019505063
- 3014204628
- 3002821232
- 3008485769
- 3030226293
- 3001452523
- 3006098219
- 2182345
- 3005260401
- 3014342096
- 1925206
- 3015286905
- 3013524663
- 3014523858
- 3007689746
- 3025460026
- 3017181414
- 3014302716
- 3011853771
- 3006553621
- 3009542966
- 3006795832
- 3027847726
- 3015005470
- 3010202439
- 3011659880
Source Documents#
510(k) summary PDF not indicated by FDA