The following data is part of a premarket notification filed by Accurate Surgical Instruments Co. with the FDA for Titanium Catheter Extender.
| Device ID | K910785 |
| 510k Number | K910785 |
| Device Name: | TITANIUM CATHETER EXTENDER |
| Classification | Catheter, Peritoneal, Long-term Indwelling |
| Applicant | ACCURATE SURGICAL INSTRUMENTS CO. 590 RICHMOND STREET WEST Toronto Canado M5v 1y9, CA M5v 1y9 |
| Contact | Helen Moreland |
| Correspondent | Helen Moreland ACCURATE SURGICAL INSTRUMENTS CO. 590 RICHMOND STREET WEST Toronto Canado M5v 1y9, CA M5v 1y9 |
| Product Code | FJS |
| CFR Regulation Number | 876.5630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-02-25 |
| Decision Date | 1991-08-22 |