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 |