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#
- 3013875443
- 3045978136
- 3030226293
- 3007218972
- 3003524740
- 3016678414
- 3031696840
- 3042262500
- 3013403214
- 1066270
- 3009567010
- 3004034546
- 3005260401
- 1824206
- 3008555994
- 3017181414
- 3016734231
- 3031082325
- 3005214422
- 3007607706
- 3010785927
- 3034755650
- 3043105505
- 3033506545
- 3009542966
- 3003781173
- 3008533516
- 3034729907
- 3043654660
- 3013685983
- 3015526491
- 1926681
- 2242467
- 2085249
- 3043460907
- 3025460026
- 3010373530
- 3014264913
- 3006098219
- 3006553621
- 3010411316
- 3006795832
- 3009273990
- 8043392
- 3015286905
- 3013354832
- 3019865493
- 3011659880
- 3006897028
- 3016162044
- 3011719874
- 3043749706
- 3010605276
- 3026311463
- 3007031016
- 3019505063
- 3009282549
- 3012709011
- 3010202439
- 3011781238
- 2432177
- 3005587124
- 3004905643
- 3021591293
- 1063324
- 3007515312
- 3030488262
- 3011647337
- 9615543
- 3016590299
- 1027229
- 3044829820
- 3004824601
- 3011853771
- 3012579728
- 3015223105
- 2529571
- 3006802326
- 3005555653
- 3008881803
Source Documents#
510(k) summary PDF not indicated by FDA