The following data is part of a premarket notification filed by Siemens Gammasonics, Inc. with the FDA for Digispot Imager.
Device ID | K871778 |
510k Number | K871778 |
Device Name: | DIGISPOT IMAGER |
Classification | Camera, Multi Format, Radiological |
Applicant | SIEMENS GAMMASONICS, INC. 2000 NUCLEAR DR. Des Plaines, IL 60018 |
Contact | Joseph P Stowell |
Correspondent | Joseph P Stowell SIEMENS GAMMASONICS, INC. 2000 NUCLEAR DR. Des Plaines, IL 60018 |
Product Code | LMC |
CFR Regulation Number | 892.2040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-05-06 |
Decision Date | 1987-05-29 |