510(k) K000927
K000927 is an FDA 510(k) premarket notification submitted by Misonix, Inc. for the device "ALLIGER ULTRASONIC SURGICAL SYSTEM MODEL AUSS-4". The FDA issued a decision of Substantially Equivalent on October 10, 2000. The device falls under product code LFL (Instrument, Ultrasonic Surgical), a Class U device. Misonix, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 10, 2000
- Date Received
- March 22, 2000
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Instrument, Ultrasonic Surgical
- Device Class
- Class U
- Regulation Number
- Review Panel
- SU
- Submission Type