The following data is part of a premarket notification filed by Cardiac Pacemakers, Inc. with the FDA for Astra T2, T4 And T6.
| Device ID | K865013 |
| 510k Number | K865013 |
| Device Name: | ASTRA T2, T4 AND T6 |
| Classification | Implantable Pacemaker Pulse-generator |
| Applicant | CARDIAC PACEMAKERS, INC. 4100 HAMLINE AVE., NORTH P.O. BOX 64079 St. Paul, MN 55112 -5798 |
| Contact | Ann H Morrissey |
| Correspondent | Ann H Morrissey CARDIAC PACEMAKERS, INC. 4100 HAMLINE AVE., NORTH P.O. BOX 64079 St. Paul, MN 55112 -5798 |
| Product Code | DXY |
| CFR Regulation Number | 870.3610 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-12-23 |
| Decision Date | 1987-02-19 |