The following data is part of a premarket notification filed by Cordis Corp. with the FDA for Right-angle Catheter For Ventricular Drainage.
| Device ID | K911433 |
| 510k Number | K911433 |
| Device Name: | RIGHT-ANGLE CATHETER FOR VENTRICULAR DRAINAGE |
| Classification | Shunt, Central Nervous System And Components |
| Applicant | CORDIS CORP. P.O. BOX 025700 Miami, FL 33102 |
| Contact | Marvin L Sussman |
| Correspondent | Marvin L Sussman CORDIS CORP. P.O. BOX 025700 Miami, FL 33102 |
| Product Code | JXG |
| CFR Regulation Number | 882.5550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-04-02 |
| Decision Date | 1991-09-16 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00382830056243 | K911433 | 000 |
| 10381780035930 | K911433 | 000 |
| 10381780035923 | K911433 | 000 |
| 10381780035916 | K911433 | 000 |
| 10381780035909 | K911433 | 000 |
| 10381780035893 | K911433 | 000 |
| 10381780035886 | K911433 | 000 |
| 10381780035879 | K911433 | 000 |
| 10381780035862 | K911433 | 000 |
| 10381780035947 | K911433 | 000 |
| 00382830055253 | K911433 | 000 |
| 00382830055970 | K911433 | 000 |
| 00382830055925 | K911433 | 000 |
| 00382830055857 | K911433 | 000 |
| 00382830055796 | K911433 | 000 |
| 00382830055697 | K911433 | 000 |
| 00382830055673 | K911433 | 000 |
| 00382830057448 | K911433 | 000 |
| 00382830055598 | K911433 | 000 |
| 10381780035855 | K911433 | 000 |