The following data is part of a premarket notification filed by Daig Corp. with the FDA for Permanent Lead Intraducer.
| Device ID | K791129 |
| 510k Number | K791129 |
| Device Name: | PERMANENT LEAD INTRADUCER |
| Classification | Introducer, Catheter |
| Applicant | DAIG CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DYB |
| CFR Regulation Number | 870.1340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-06-14 |
| Decision Date | 1979-07-17 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 15415067021042 | K791129 | 000 |
| 15414734204597 | K791129 | 000 |
| 05414734204415 | K791129 | 000 |
| 05414734204408 | K791129 | 000 |
| 05414734204392 | K791129 | 000 |
| 05414734204385 | K791129 | 000 |
| 05414734204378 | K791129 | 000 |
| 05414734204361 | K791129 | 000 |
| 15414734204245 | K791129 | 000 |
| 15414734204221 | K791129 | 000 |
| 15414734204207 | K791129 | 000 |
| 15414734204160 | K791129 | 000 |
| 15414734204146 | K791129 | 000 |
| 15414734204122 | K791129 | 000 |
| 15414734204702 | K791129 | 000 |
| 15414734204726 | K791129 | 000 |
| 15415067021035 | K791129 | 000 |
| 15415067021028 | K791129 | 000 |
| 15415067021011 | K791129 | 000 |
| 15415067021004 | K791129 | 000 |
| 15415067020953 | K791129 | 000 |
| 15415067020946 | K791129 | 000 |
| 15415067020939 | K791129 | 000 |
| 15415067020915 | K791129 | 000 |
| 15414734204979 | K791129 | 000 |
| 15414734204931 | K791129 | 000 |
| 15414734204894 | K791129 | 000 |
| 15414734204870 | K791129 | 000 |
| 15414734204856 | K791129 | 000 |
| 15414734204108 | K791129 | 000 |