510(k) K013417
K013417 is an FDA 510(k) premarket notification submitted by Misonix, Inc. for the device "MISONIX IRRIGATION SYSTEM MOEDL BC20P". The FDA issued a decision of Substantially Equivalent on January 10, 2002. The device falls under product code GBX (Catheter, Irrigation), a Class I device regulated under 21 CFR 878.4200. Misonix, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 10, 2002
- Date Received
- October 15, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Irrigation
- Device Class
- Class I
- Regulation Number
- 878.4200
- Review Panel
- SU
- Submission Type