The following data is part of a premarket notification filed by Clinical Neuro Systems Llc. with the FDA for Clinical Neuro Systems Monitorr Icp Ventricular Ca.
Device ID | K922941 |
510k Number | K922941 |
Device Name: | CLINICAL NEURO SYSTEMS MONITORR ICP VENTRICULAR CA |
Classification | Shunt, Central Nervous System And Components |
Applicant | CLINICAL NEURO SYSTEMS LLC. 875 NORMA WAY Santa Barbara, CA 93111 |
Contact | Stephen W Laguette |
Correspondent | Stephen W Laguette CLINICAL NEURO SYSTEMS LLC. 875 NORMA WAY Santa Barbara, CA 93111 |
Product Code | JXG |
CFR Regulation Number | 882.5550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-06-18 |
Decision Date | 1992-08-26 |