K870460 is an FDA 510(k) clearance for the DORROS(TM) SMALL VESSEL PTA CATHETER. This device is classified as a System, Measurement, Blood-pressure, Non-invasive (Class II - Special Controls, product code DXN).
Submitted by C.R. Bard, Inc. (Murray Hill, US). The FDA issued a Cleared decision on June 5, 1987, 122 days after receiving the submission on February 3, 1987.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1130.
| 510(k) Number | K870460 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 03, 1987 |
| Decision Date | June 05, 1987 |
| Days to Decision | 122 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | — |
| Product Code | DXN — System, Measurement, Blood-pressure, Non-invasive |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1130 |