K890807 is an FDA 510(k) clearance for the GUIDE WIRE INTRODUCER. This device is classified as a Wire, Guide, Catheter (Class II - Special Controls, product code DQX).
Submitted by Datascope Corp. (Oakland, US). The FDA issued a Cleared decision on June 20, 1989, 124 days after receiving the submission on February 16, 1989.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1330.
| 510(k) Number | K890807 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 16, 1989 |
| Decision Date | June 20, 1989 |
| Days to Decision | 124 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | - |
| Product Code | DQX - Wire, Guide, Catheter |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1330 |