The following data is part of a premarket notification filed by Physiometrix, Inc. with the FDA for Model 1207, Hydrodot Neuromonitoring System Adhesive Pads.
Device ID | K953449 |
510k Number | K953449 |
Device Name: | MODEL 1207, HYDRODOT NEUROMONITORING SYSTEM ADHESIVE PADS |
Classification | Full-montage Standard Electroencephalograph |
Applicant | PHYSIOMETRIX, INC. FIVE BILLERICA PARK 101 BILLERICA AVENUE North Billerica, MA 01862 |
Contact | Dawn E Frazer |
Correspondent | Dawn E Frazer PHYSIOMETRIX, INC. FIVE BILLERICA PARK 101 BILLERICA AVENUE North Billerica, MA 01862 |
Product Code | GWQ |
CFR Regulation Number | 882.1400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-07-18 |
Decision Date | 1995-10-12 |