The following data is part of a premarket notification filed by Bio-logic Systems Corp. with the FDA for Bio-logic Sleepscan Product With Built-in Oximeter.
Device ID | K962103 |
510k Number | K962103 |
Device Name: | BIO-LOGIC SLEEPSCAN PRODUCT WITH BUILT-IN OXIMETER |
Classification | Ventilatory Effort Recorder |
Applicant | BIO-LOGIC SYSTEMS CORP. ONE BIO-LOGIC PLAZA Mundelein, IL 60060 -3700 |
Contact | Norman E Brunner |
Correspondent | Norman E Brunner BIO-LOGIC SYSTEMS CORP. ONE BIO-LOGIC PLAZA Mundelein, IL 60060 -3700 |
Product Code | MNR |
CFR Regulation Number | 868.2375 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-05-30 |
Decision Date | 1996-08-22 |
Summary: | summary |