The following data is part of a premarket notification filed by Daig Corp. with the FDA for Daig Diagnostic Electrophysiology Catheter.
| Device ID | K942379 |
| 510k Number | K942379 |
| Device Name: | DAIG DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER |
| Classification | Catheter, Electrode Recording, Or Probe, Electrode Recording |
| Applicant | DAIG CORP. 14901 DEVEAU PLACE Minnetonka, MN 55345 -2126 |
| Contact | John J Fleischhacker |
| Correspondent | John J Fleischhacker DAIG CORP. 14901 DEVEAU PLACE Minnetonka, MN 55345 -2126 |
| Product Code | DRF |
| CFR Regulation Number | 870.1220 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-05-09 |
| Decision Date | 1994-12-27 |