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#
- 3005651859
- 3007123908
- 3006795832
- 3009425497
- 3043749706
- 3030516433
- 1422443
- 3014172160
- 9610617
- 3013875443
- 3034535
- 3013495708
- 3006098219
- 3016096058
- 3016162044
- 3039527731
- 3009952786
- 3010373263
- 3015526491
- 3012709011
- 3010675897
- 3039065815
- 1063324
- 3038623066
- 3013354832
- 3005545844
- 3010605307
- 3009282549
- 3033882216
- 3009542966
- 1000122786
- 3014302716
- 3008386649
- 3033849261
- 3010373530
- 3010707607
- 3004034546
- 3013685983
- 1027229
- 3011853771
- 9613910
- 3031696840
- 3013831261
- 3016678414
- 3014471045
- 3006553621
- 3005214422
- 3012316249
- 3029983606
- 3012579728
- 3027643666
- 3027332478
- 3007218972
- 3010564728
- 3010785927
- 3027847726
- 3005260401
- 1836161
- 3006802326
- 3037012186
- 3043105505
- 3033433849
- 3015536186
- 8022890
- 3011719874
- 3043128491
- 3020188747
- 3038191348
- 3005555653
- 3011574775
- 3007278668
- 3008881803
- 9615415
- 3019865493
- 2529571
- 3031582440
- 3004905643
- 3014523858
- 3015058854
Source Documents#
510(k) summary PDF not indicated by FDA