510(k) K930221
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