The following data is part of a premarket notification filed by Stellate Systems with the FDA for Harmone-schwarzer Eeg System.
Device ID | K010728 |
510k Number | K010728 |
Device Name: | HARMONE-SCHWARZER EEG SYSTEM |
Classification | Standard Polysomnograph With Electroencephalograph |
Applicant | STELLATE SYSTEMS 345 VICTORIA AVE., SUITE 300 Westmount, Quebec, CA H3z 2n2 |
Contact | George Papagiannis |
Correspondent | George Papagiannis STELLATE SYSTEMS 345 VICTORIA AVE., SUITE 300 Westmount, Quebec, CA H3z 2n2 |
Product Code | OLV |
CFR Regulation Number | 882.1400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-03-12 |
Decision Date | 2001-05-21 |