The following data is part of a premarket notification filed by Endosonics Corp. with the FDA for Resolve Option For The Oracle In Vision Intravascular Ultrasonic Imaging System.
| Device ID | K965223 |
| 510k Number | K965223 |
| Device Name: | RESOLVE OPTION FOR THE ORACLE IN VISION INTRAVASCULAR ULTRASONIC IMAGING SYSTEM |
| Classification | System, Imaging, Pulsed Echo, Ultrasonic |
| Applicant | ENDOSONICS CORP. 2870 KILGORE RD. Rancho Cordova, CA 95670 |
| Contact | Adam Savakus |
| Correspondent | Adam Savakus ENDOSONICS CORP. 2870 KILGORE RD. Rancho Cordova, CA 95670 |
| Product Code | IYO |
| CFR Regulation Number | 892.1560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-12-31 |
| Decision Date | 1998-06-29 |
| Summary: | summary |