510(k) K930221

CAMINO VENTRICULAR TRANSDUCER ACCESSORY by Camino Laboratories, Inc. — Product Code GWM

K930221 is an FDA 510(k) premarket notification submitted by Camino Laboratories, Inc. for the device "CAMINO VENTRICULAR TRANSDUCER ACCESSORY". The FDA issued a decision of Substantially Equivalent on April 15, 1993. The device falls under product code GWM (Device, Monitoring, Intracranial Pressure), a Class II device regulated under 21 CFR 882.1620. Camino Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 15, 1993
Date Received
January 15, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Monitoring, Intracranial Pressure
Device Class
Class II
Regulation Number
882.1620
Review Panel
NE
Submission Type