The following data is part of a premarket notification filed by Cordis Corp. with the FDA for Cordis Catheter Sheath Introducer.
| Device ID | K932733 |
| 510k Number | K932733 |
| Device Name: | CORDIS CATHETER SHEATH INTRODUCER |
| Classification | Introducer, Catheter |
| Applicant | CORDIS CORP. 14201 N.W. 60TH AVE. Miami Lakes, FL 33014 |
| Contact | David Kornhauser |
| Correspondent | David Kornhauser CORDIS CORP. 14201 N.W. 60TH AVE. Miami Lakes, FL 33014 |
| Product Code | DYB |
| CFR Regulation Number | 870.1340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-06-07 |
| Decision Date | 1993-08-26 |