The following data is part of a premarket notification filed by Y with the FDA for Intravascular Administration Set.
| Device ID | K790582 |
| 510k Number | K790582 |
| Device Name: | INTRAVASCULAR ADMINISTRATION SET |
| Classification | Set, Administration, Intravascular |
| Applicant | Y 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-03-27 |
| Decision Date | 1979-05-29 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 50885403278356 | K790582 | 000 |
| 50885403222618 | K790582 | 000 |
| 50885403222601 | K790582 | 000 |
| 50885403221932 | K790582 | 000 |
| 50885403221925 | K790582 | 000 |
| 50885403221840 | K790582 | 000 |
| 50885403198913 | K790582 | 000 |
| 37613203010086 | K790582 | 000 |
| 37613203009547 | K790582 | 000 |
| 50885403225626 | K790582 | 000 |
| 50885403226128 | K790582 | 000 |
| 50885403229921 | K790582 | 000 |
| 50885403240995 | K790582 | 000 |
| 50885403240865 | K790582 | 000 |
| 50885403235731 | K790582 | 000 |
| 50885403235465 | K790582 | 000 |
| 50885403234758 | K790582 | 000 |
| 50885403234741 | K790582 | 000 |
| 50885403230118 | K790582 | 000 |
| 50885403229938 | K790582 | 000 |
| 37613203009462 | K790582 | 000 |