The following data is part of a premarket notification filed by Sheridan Catheter Corp. with the FDA for Sheridan/endo-pak.
| Device ID | K842635 |
| 510k Number | K842635 |
| Device Name: | SHERIDAN/ENDO-PAK |
| Classification | Tube, Tracheal (w/wo Connector) |
| Applicant | SHERIDAN CATHETER CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BTR |
| CFR Regulation Number | 868.5730 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-07-09 |
| Decision Date | 1984-07-25 |