The following data is part of a premarket notification filed by Bio-logic Systems Corp. with the FDA for Bio-logic Master Ii Evoked Response System.
Device ID | K073626 |
510k Number | K073626 |
Device Name: | BIO-LOGIC MASTER II EVOKED RESPONSE SYSTEM |
Classification | Stimulator, Auditory, Evoked Response |
Applicant | BIO-LOGIC SYSTEMS CORP. ONE BIOLOGIC PLAZA Mundelein, IL 60060 |
Contact | Nicohl Wilding |
Correspondent | Nicohl Wilding BIO-LOGIC SYSTEMS CORP. ONE BIOLOGIC PLAZA Mundelein, IL 60060 |
Product Code | GWJ |
CFR Regulation Number | 882.1900 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-12-26 |
Decision Date | 2008-02-05 |
Summary: | summary |