K982406 is an FDA 510(k) clearance for the COBE VACUUM RELIEF CHECK VALVE. This device is classified as a Cpb Check Valve, Retrograde Flow, In-line (Class II - Special Controls, product code MJJ).
Submitted by Cobe Cardiovascular, Inc. (Arvada, US). The FDA issued a Cleared decision on October 7, 1998, 89 days after receiving the submission on July 10, 1998.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.4400.
| 510(k) Number | K982406 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 10, 1998 |
| Decision Date | October 07, 1998 |
| Days to Decision | 89 days |
| Submission Type | Abbreviated |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | MJJ — Cpb Check Valve, Retrograde Flow, In-line |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.4400 |