The following data is part of a premarket notification filed by J. Morita Usa, Inc. with the FDA for 3d Accu-i-tomo Xyz Slice View Tomograph.
Device ID | K030450 |
510k Number | K030450 |
Device Name: | 3D ACCU-I-TOMO XYZ SLICE VIEW TOMOGRAPH |
Classification | System, X-ray, Tomography, Computed |
Applicant | J. MORITA USA, INC. 1425 K ST. N.W. SUITE 1100 Washington, DC 20005 |
Contact | Keith A Barritt |
Correspondent | Keith A Barritt J. MORITA USA, INC. 1425 K ST. N.W. SUITE 1100 Washington, DC 20005 |
Product Code | JAK |
CFR Regulation Number | 892.1750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-02-11 |
Decision Date | 2003-05-06 |
Summary: | summary |