The following data is part of a premarket notification filed by Ohmeda Medical with the FDA for Diprivan Luer Connector.
| Device ID | K935274 |
| 510k Number | K935274 |
| Device Name: | DIPRIVAN LUER CONNECTOR |
| Classification | Set, I.v. Fluid Transfer |
| Applicant | OHMEDA MEDICAL 2007 PAN AM CIRCLE Tampa, FL 33702 |
| Contact | Rachel J Swatridge |
| Correspondent | Rachel J Swatridge OHMEDA MEDICAL 2007 PAN AM CIRCLE Tampa, FL 33702 |
| Product Code | LHI |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-11-03 |
| Decision Date | 1994-03-15 |