K894157 is an FDA 510(k) clearance for the OBTURATOR. This device is classified as a Introducer, Catheter (Class II - Special Controls, product code DYB).
Submitted by Argon Medical Corp. (Athens, US). The FDA issued a Cleared decision on September 28, 1989, 106 days after receiving the submission on June 14, 1989.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1340.
| 510(k) Number | K894157 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 14, 1989 |
| Decision Date | September 28, 1989 |
| Days to Decision | 106 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | — |
| Product Code | DYB — Introducer, Catheter |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1340 |