K890785 is an FDA 510(k) clearance for the ASTRA T2, T3, T4, T6 PULSE GENERATORS NEW PACKAGE. This device is classified as a Implantable Pacemaker Pulse-generator (Class III - Premarket Approval, product code DXY).
Submitted by Cardiac Pacemakers, Inc. (St. Paul, US). The FDA issued a Cleared decision on March 10, 1989, 23 days after receiving the submission on February 15, 1989.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.3610.
| 510(k) Number | K890785 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 15, 1989 |
| Decision Date | March 10, 1989 |
| Days to Decision | 23 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | — |
| Product Code | DXY — Implantable Pacemaker Pulse-generator |
| Device Class | Class III - Premarket Approval |
| CFR Regulation | 21 CFR 870.3610 |