The following data is part of a premarket notification filed by Image-guided Neurologics, Inc. with the FDA for Active Array Catheter, Model Cs-2000.
Device ID | K001097 |
510k Number | K001097 |
Device Name: | ACTIVE ARRAY CATHETER, MODEL CS-2000 |
Classification | Coil, Magnetic Resonance, Specialty |
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 | MOS |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-04-04 |
Decision Date | 2001-01-18 |