The following data is part of a premarket notification filed by Vertex Medical Corp. with the FDA for Nephrostomy/biliary Drainage Bag.
| Device ID | K834476 |
| 510k Number | K834476 |
| Device Name: | NEPHROSTOMY/BILIARY DRAINAGE BAG |
| Classification | Catheter, Nephrostomy |
| Applicant | VERTEX MEDICAL CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LJE |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-12-20 |
| Decision Date | 1984-02-04 |