The following data is part of a premarket notification filed by Medsurg Industries, Inc. with the FDA for 7 Fr. Triple Lumen Central Vein Catheteri. System.
| Device ID | K880776 |
| 510k Number | K880776 |
| Device Name: | 7 FR. TRIPLE LUMEN CENTRAL VEIN CATHETERI. SYSTEM |
| Classification | Cannula, Catheter |
| 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 | DQR |
| CFR Regulation Number | 870.1300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-02-26 |
| Decision Date | 1988-05-02 |