The following data is part of a premarket notification filed by Cordis Corp. with the FDA for Cordis Polypropylene Straight, T & Y Connector.
| Device ID | K921936 |
| 510k Number | K921936 |
| Device Name: | CORDIS POLYPROPYLENE STRAIGHT, T & Y CONNECTOR |
| 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 | 1992-04-24 |
| Decision Date | 1992-10-30 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00382830057462 | K921936 | 000 |
| 10381780034636 | K921936 | 000 |
| 10381780034643 | K921936 | 000 |
| 10381780034650 | K921936 | 000 |
| 10381780034667 | K921936 | 000 |
| 00382830057479 | K921936 | 000 |
| 00382830057486 | K921936 | 000 |
| 00382830057493 | K921936 | 000 |
| 00382830057455 | K921936 | 000 |
| 10381780034629 | K921936 | 000 |