The following data is part of a premarket notification filed by Oximetrix, Inc. with the FDA for Opticath Heparin Coated, Flow-direct.
| Device ID | K823007 |
| 510k Number | K823007 |
| Device Name: | OPTICATH HEPARIN COATED, FLOW-DIRECT |
| Classification | Catheter, Flow Directed |
| Applicant | OXIMETRIX, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DYG |
| CFR Regulation Number | 870.1240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-10-12 |
| Decision Date | 1982-11-01 |