The following data is part of a premarket notification filed by Cordis Corp. with the FDA for Cordis Cinch(r) Steerable Guidewire Ext W/slx Coat.
| Device ID | K914863 |
| 510k Number | K914863 |
| Device Name: | CORDIS CINCH(R) STEERABLE GUIDEWIRE EXT W/SLX COAT |
| Classification | Wire, Guide, Catheter |
| Applicant | CORDIS CORP. 14201 N.W. 60TH AVE. Miami Lakes, FL 33014 |
| Contact | Katherine Trevisol |
| Correspondent | Katherine Trevisol CORDIS CORP. 14201 N.W. 60TH AVE. Miami Lakes, FL 33014 |
| Product Code | DQX |
| CFR Regulation Number | 870.1330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-10-29 |
| Decision Date | 1991-12-18 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20705032009567 | K914863 | 000 |