The following data is part of a premarket notification filed by Ohmeda Medical with the FDA for Viggo Vascuport Needle.
| Device ID | K881758 |
| 510k Number | K881758 |
| Device Name: | VIGGO VASCUPORT NEEDLE |
| Classification | Needle, Hypodermic, Single Lumen |
| Applicant | OHMEDA MEDICAL 2007 PAN AM CIRCLE Tampa, FL 33702 |
| Contact | Jill Phillips |
| Correspondent | Jill Phillips OHMEDA MEDICAL 2007 PAN AM CIRCLE Tampa, FL 33702 |
| Product Code | FMI |
| CFR Regulation Number | 880.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-04-25 |
| Decision Date | 1988-06-03 |