The following data is part of a premarket notification filed by American Edwards Laboratories with the FDA for Nephrostomy Drainage Catheter & Stiffener.
| Device ID | K845048 |
| 510k Number | K845048 |
| Device Name: | NEPHROSTOMY DRAINAGE CATHETER & STIFFENER |
| Classification | Catheter, Nephrostomy |
| Applicant | AMERICAN EDWARDS LABORATORIES P.O. BOX 11150 17221 RED HILL AVE.(IRVINE) Santa Ana, CA 92711 -1150 |
| Contact | Ronald J Ehmsen |
| Correspondent | Ronald J Ehmsen AMERICAN EDWARDS LABORATORIES P.O. BOX 11150 17221 RED HILL AVE.(IRVINE) Santa Ana, CA 92711 -1150 |
| 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 | 1984-12-31 |
| Decision Date | 1985-01-15 |