The following data is part of a premarket notification filed by Onset Medical Corporation with the FDA for Pathway Ureteral Access Sheath, Pathway Expandable Ureteral Access Sheath.
| Device ID | K043254 |
| 510k Number | K043254 |
| Device Name: | PATHWAY URETERAL ACCESS SHEATH, PATHWAY EXPANDABLE URETERAL ACCESS SHEATH |
| Classification | Dilator, Catheter, Ureteral |
| Applicant | ONSET MEDICAL CORPORATION 27001 LA PAZ SUITE 312 Mission Viejo, CA 92691 |
| Contact | Albert Rego |
| Correspondent | Albert Rego ONSET MEDICAL CORPORATION 27001 LA PAZ SUITE 312 Mission Viejo, CA 92691 |
| Product Code | EZN |
| CFR Regulation Number | 876.5470 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-11-24 |
| Decision Date | 2005-02-10 |