The following data is part of a premarket notification filed by Sheridan Catheter Corp. with the FDA for Sheri-i-slip Intubating Stylet.
| Device ID | K832773 |
| 510k Number | K832773 |
| Device Name: | SHERI-I-SLIP INTUBATING STYLET |
| Classification | Stylet, Tracheal Tube |
| Applicant | SHERIDAN CATHETER CORP. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | BSR |
| CFR Regulation Number | 868.5790 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-08-16 |
| Decision Date | 1983-09-12 |