510(k) K896211
K896211 is an FDA 510(k) premarket notification submitted by Westmark, Sterile Packing Systems, Inc. (Sps) for the device "CYSTOSCOPY/IRRIGATION SET". The FDA issued a decision of Substantially Equivalent on January 18, 1990. The device falls under product code KOD (Catheter, Urological), a Class II device regulated under 21 CFR 876.5130. Westmark, Sterile Packing Systems, Inc. (Sps) has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 18, 1990
- Date Received
- October 26, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Urological
- Device Class
- Class II
- Regulation Number
- 876.5130
- Review Panel
- GU
- Submission Type