The following data is part of a premarket notification filed by Medsurg Industries, Inc. with the FDA for Continuous Arterial/venous Hemofiltration Tray.
| Device ID | K880775 |
| 510k Number | K880775 |
| Device Name: | CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION TRAY |
| Classification | Catheter, Femoral |
| Applicant | MEDSURG INDUSTRIES, INC. 251 EXCHANGE PLACE Herndon, VA 20170 -4822 |
| Contact | Tom Bonner |
| Correspondent | Tom Bonner MEDSURG INDUSTRIES, INC. 251 EXCHANGE PLACE Herndon, VA 20170 -4822 |
| Product Code | LFK |
| CFR Regulation Number | 876.5540 [🔎] |
| Decision | Substantially Equivalent - With Drug (SESD) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-02-26 |
| Decision Date | 1988-07-25 |