The following data is part of a premarket notification filed by Namic with the FDA for Arterial Extension Set.
| Device ID | K790082 |
| 510k Number | K790082 |
| Device Name: | ARTERIAL EXTENSION SET |
| Classification | Catheter, Intravascular, Diagnostic |
| Applicant | NAMIC 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DQO |
| CFR Regulation Number | 870.1200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-01-12 |
| Decision Date | 1979-01-25 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10193489067095 | K790082 | 000 |
| 20193489064596 | K790082 | 000 |
| 20193489064602 | K790082 | 000 |
| 20193489064619 | K790082 | 000 |
| 20193489064626 | K790082 | 000 |
| 20193489068464 | K790082 | 000 |
| 20193489068471 | K790082 | 000 |
| 20193489068488 | K790082 | 000 |
| 20193489068495 | K790082 | 000 |
| 10193489087789 | K790082 | 000 |
| 20193489067603 | K790082 | 000 |
| 20193489067627 | K790082 | 000 |
| 20193489067610 | K790082 | 000 |
| 20193489067078 | K790082 | 000 |
| 20193489064589 | K790082 | 000 |