K960575 is an FDA 510(k) clearance for the ADVANTX LCV+. This device is classified as a System, X-ray, Angiographic (Class II - Special Controls, product code IZI).
Submitted by GE Medical Systems (Milwaukee, US). The FDA issued a Cleared decision on May 7, 1996, 85 days after receiving the submission on February 12, 1996.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1600.
| 510(k) Number | K960575 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 12, 1996 |
| Decision Date | May 07, 1996 |
| Days to Decision | 85 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | IZI - System, X-ray, Angiographic |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1600 |