510(k) K943361
K943361 is an FDA 510(k) premarket notification submitted by Northgate Technologies, Inc. for the device "NORTHGATE FLOW ASSIST TUBING FOR UROLOGY". The FDA issued a decision of Substantially Equivalent on September 29, 1995. The device falls under product code LJH (System, Irrigation, Urological), a Class II device regulated under 21 CFR 876.5130. Northgate Technologies, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 29, 1995
- Date Received
- July 13, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Irrigation, Urological
- Device Class
- Class II
- Regulation Number
- 876.5130
- Review Panel
- GU
- Submission Type