The following data is part of a premarket notification filed by Sil-med Corp. with the FDA for Trudell Bent Catheter.
| Device ID | K885167 |
| 510k Number | K885167 |
| Device Name: | TRUDELL BENT CATHETER |
| Classification | Catheter, Peritoneal, Long-term Indwelling |
| Applicant | SIL-MED CORP. 700 WARNER BLVD. Taunton, MA 02780 |
| Contact | S Mccallum |
| Correspondent | S Mccallum SIL-MED CORP. 700 WARNER BLVD. Taunton, MA 02780 |
| Product Code | FJS |
| CFR Regulation Number | 876.5630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-12-13 |
| Decision Date | 1989-01-31 |