510(k) K942875
- Device
- Model #900to3500 Head/neck Coil
- Applicant
- MEDIC, INC.
- 510(k) number
- K942875
- Product code
- LNH
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1994-12-02
- Date received
- 1994-06-17
- Regulation
- 892.1000
- Classification name
- System, Nuclear Magnetic Resonance Imaging
- Medical specialty
- Radiology
- Review panel
- Radiology
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Statement
- Third party reviewed
- No
Applicant Contact#
- Contact
- RANDALL W JONES
- Address
- 925 W. 6th St. P.O. Box 737 Fremont NE US 68025 68025
FDA Registration Numbers#
- 3009715136
- 3013679558
- 3006849754
- 3009963139
- 1319639
- 3008284470
- 3017375271
- 3015431711
- 3042177665
- 3025602463
- 3009882464
- 3005976071
- 3014635027
- 9611343
- 3032109181
- 3010009632
- 3003661577
- 3006073271
- 3010701021
- 3008986341
- 3009196578
- 3013343065
- 3010703925
- 3008355361
- 3007350713
- 3009714754
- 3004929307
- 3014809646
- 3018004899
- 9616047
- 3012075008
- 3007546534
- 3011015597
- 3011657336
- 2126677
- 3009504230
- 3008632256
- 3030982377
- 2432211
- 3012085143
- 3006015847
- 1054713
- 3016591365
- 3021593788
- 3010398867
- 3033333119
- 2520313
- 3019595609
- 3016727312
- 3023003446
- 3011767965
- 3007734888
- 3027325776
- 3012439308
- 1650907
- 2183553
- 3014343100
- 3015276088
- 3012761544
- 3027339477
- 3015223550
- 3036666444
- 3032109225
- 3006621332
- 3016851825
- 3035950510
- 3015425142
- 9617016
- 3007562060
- 3004531751
- 3009154005
- 3029521953
- 3031503890
- 3009077524
- 3011950073
- 3005326970
- 1826555
- 3012127758
- 3034286426
Source Documents#
510(k) summary PDF not indicated by FDA
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