The following data is part of a premarket notification filed by Elscint, Inc. with the FDA for Elscint's Exel 2400e Ct Scanner.
Device ID | K894542 |
510k Number | K894542 |
Device Name: | ELSCINT'S EXEL 2400E CT SCANNER |
Classification | System, X-ray, Tomography, Computed |
Applicant | ELSCINT, INC. 505 MAIN ST. SUITE 300 Hackensack, NJ 07601 |
Contact | Rochelle M Sobel |
Correspondent | Rochelle M Sobel ELSCINT, INC. 505 MAIN ST. SUITE 300 Hackensack, NJ 07601 |
Product Code | JAK |
CFR Regulation Number | 892.1750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-07-20 |
Decision Date | 1989-09-07 |