The following data is part of a premarket notification filed by Y with the FDA for 30-30-2 700 Syringe Extension Set.
| Device ID | K811885 |
| 510k Number | K811885 |
| Device Name: | 30-30-2 700 SYRINGE EXTENSION 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 | 1981-07-01 |
| Decision Date | 1981-08-25 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 50885403274006 | K811885 | 000 |
| 50885403234369 | K811885 | 000 |
| 50885403234352 | K811885 | 000 |
| 50885403234260 | K811885 | 000 |
| 50885403234185 | K811885 | 000 |
| 50885403234048 | K811885 | 000 |
| 50885403233942 | K811885 | 000 |
| 50885403233935 | K811885 | 000 |
| 50885403233928 | K811885 | 000 |
| 50885403233911 | K811885 | 000 |
| 50885403233904 | K811885 | 000 |
| 50885403233898 | K811885 | 000 |
| 50885403233799 | K811885 | 000 |
| 50885403234376 | K811885 | 000 |
| 50885403234383 | K811885 | 000 |
| 50885403273993 | K811885 | 000 |
| 50885403273955 | K811885 | 000 |
| 50885403273948 | K811885 | 000 |
| 50885403235243 | K811885 | 000 |
| 50885403235236 | K811885 | 000 |
| 50885403235229 | K811885 | 000 |
| 50885403235212 | K811885 | 000 |
| 50885403234604 | K811885 | 000 |
| 50885403234420 | K811885 | 000 |
| 50885403234413 | K811885 | 000 |
| 50885403234406 | K811885 | 000 |
| 50885403234390 | K811885 | 000 |
| 50885403233485 | K811885 | 000 |