510(k) K942688
K942688 is an FDA 510(k) premarket notification submitted by Uresil Corp. for the device "NEPHRO-URETERAL STENT". The FDA issued a decision of Substantially Equivalent on June 6, 1995. The device falls under product code LJE (Catheter, Nephrostomy), a Class U device. Uresil Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 6, 1995
- Date Received
- June 7, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Nephrostomy
- Device Class
- Class U
- Regulation Number
- Review Panel
- GU
- Submission Type