K820702 is an FDA 510(k) clearance for the IL 7F FLOW DIRECTOR THERMAL DILU. CATH. This device is classified as a Catheter, Flow Directed (Class II - Special Controls, product code DYG).
Submitted by Instrumentation Laboratory CO (Mchenry, US). The FDA issued a Cleared decision on April 21, 1982, 37 days after receiving the submission on March 15, 1982.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1240.
| 510(k) Number | K820702 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 15, 1982 |
| Decision Date | April 21, 1982 |
| Days to Decision | 37 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | — |
| Product Code | DYG — Catheter, Flow Directed |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1240 |