510(k) K092250
K092250 is an FDA 510(k) premarket notification submitted by Medline Industries, Inc. for the device "MEDLINE RED RUBBER URETHRAL CATHETER". The FDA issued a decision of Substantially Equivalent on January 21, 2010. The device falls under product code EYB (Catheter, Ureteral, Gastro-Urology), a Class II device regulated under 21 CFR 876.5130. Medline Industries, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 21, 2010
- Date Received
- July 28, 2009
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Ureteral, Gastro-Urology
- Device Class
- Class II
- Regulation Number
- 876.5130
- Review Panel
- GU
- Submission Type