510(k) K024050
K024050 is an FDA 510(k) premarket notification submitted by Cook Urological, Inc. for the device "COOK NEPHROSTOMY DILATION BALLOON CATHETER SET". The FDA issued a decision of Substantially Equivalent on February 27, 2003. The device falls under product code LJE (Catheter, Nephrostomy), a Class U device. Cook Urological, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 27, 2003
- Date Received
- December 9, 2002
- 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