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#
- 3038623066
- 1831748
- 3017278503
- 2432177
- 3009591865
- 3013831261
- 2020550
- 1836161
- 3033506545
- 3010785927
- 3016678950
- 3043128491
- 3010394125
- 3014302716
- 3011621895
- 3012316249
- 3013354832
- 3039527731
- 3034535
- 3037012186
- 3013903013
- 9618009
- 3014523858
- 3015286905
- 8022890
- 3012579728
- 3043749706
- 3009273990
- 3008386649
- 3014739961
- 3014204628
- 3004824601
- 9615010
- 3035641086
- 3007689746
- 3019865493
- 3014471045
- 3009157571
- 3006795832
- 3030558088
- 3031696840
- 3009952786
- 3007913191
- 3003524740
- 3027643666
- 3017171467
- 9616086
- 3004186402
- 2085249
- 3043654660
- 3007278668
- 3010605276
- 3045978136
- 3017264244
- 3033882216
- 3003781173
- 3006098219
- 3025460026
- 1925206
- 3005214422
- 1066270
- 3020188747
- 3009408502
- 3035641505
- 3004034546
- 1000122786
- 3014810929
- 3043105505
- 3010411316
- 3029983606
- 3008881803
- 3013495708
- 3013685983
- 3004194020
- 3031082325
- 3007518294
- 3039065815
- 3011574775
- 3016915446
- 3016590299
Source Documents#
510(k) summary PDF not indicated by FDA