The following data is part of a premarket notification filed by Image-guided Neurologics, Inc. with the FDA for Navigus Peel Away Introducer.
Device ID | K002330 |
510k Number | K002330 |
Device Name: | NAVIGUS PEEL AWAY INTRODUCER |
Classification | Endoscope, Neurological |
Applicant | IMAGE-GUIDED NEUROLOGICS, INC. 2290 EAU GALLIE BLVD. Melbourne, FL 32935 |
Contact | David M Lee |
Correspondent | David M Lee IMAGE-GUIDED NEUROLOGICS, INC. 2290 EAU GALLIE BLVD. Melbourne, FL 32935 |
Product Code | GWG |
CFR Regulation Number | 882.1480 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-08-01 |
Decision Date | 2000-10-18 |