The following data is part of a premarket notification filed by Elscint, Inc. with the FDA for Apex 215m Mobile Anger Camera.
Device ID | K884673 |
510k Number | K884673 |
Device Name: | APEX 215M MOBILE ANGER CAMERA |
Classification | Camera, Scintillation (gamma) |
Applicant | ELSCINT, INC. 930 COMMONWEALTH AVE. Boston, MA 02215 |
Contact | Sobel |
Correspondent | Sobel ELSCINT, INC. 930 COMMONWEALTH AVE. Boston, MA 02215 |
Product Code | IYX |
CFR Regulation Number | 892.1100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-11-08 |
Decision Date | 1989-04-14 |