510(k) K932094
K932094 is an FDA 510(k) premarket notification submitted by Mdt Corp., Inc. for the device "BOVIE ULTRASONIC SURGICAL ASPIRATOR". The FDA issued a decision of Substantially Equivalent on July 21, 1993. The device falls under product code LFL (Instrument, Ultrasonic Surgical), a Class U device. Mdt Corp., Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 21, 1993
- Date Received
- April 30, 1993
- 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