The following data is part of a premarket notification filed by Ics Medical Corp. with the FDA for Chartr Ep.
Device ID | K960097 |
510k Number | K960097 |
Device Name: | CHARTR EP |
Classification | Stimulator, Auditory, Evoked Response |
Applicant | ICS MEDICAL CORP. 2227 HAMMOND DR. Schaumburg, IL 60173 -3860 |
Contact | Delmar F Bloem |
Correspondent | Delmar F Bloem ICS MEDICAL CORP. 2227 HAMMOND DR. Schaumburg, IL 60173 -3860 |
Product Code | GWJ |
CFR Regulation Number | 882.1900 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-01-11 |
Decision Date | 1997-02-21 |