The following data is part of a premarket notification filed by Civco Medical Instruments with the FDA for Ultrasound General Purpose Guidance System.
Device ID | K093713 |
510k Number | K093713 |
Device Name: | ULTRASOUND GENERAL PURPOSE GUIDANCE SYSTEM |
Classification | Transducer, Ultrasonic, Diagnostic |
Applicant | CIVCO MEDICAL INSTRUMENTS 962 ALLEGRO LANE Apollo Beach, FL 33572 |
Contact | Arthur Ward |
Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
Product Code | ITX |
CFR Regulation Number | 892.1570 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2009-12-01 |
Decision Date | 2010-01-19 |
Summary: | summary |