The following data is part of a premarket notification filed by Civco with the FDA for Etrax Needle System, Etrax Variable Angle Needle Guidance System, Virtutrax Universal Tracker.
Device ID | K092619 |
510k Number | K092619 |
Device Name: | ETRAX NEEDLE SYSTEM, ETRAX VARIABLE ANGLE NEEDLE GUIDANCE SYSTEM, VIRTUTRAX UNIVERSAL TRACKER |
Classification | System, Imaging, Pulsed Echo, Ultrasonic |
Applicant | CIVCO 102 FIRST ST. SOUTH Kalona, IA 52247 |
Contact | James Leong |
Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
Product Code | IYO |
CFR Regulation Number | 892.1560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2009-08-26 |
Decision Date | 2009-11-13 |
Summary: | summary |