510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K932094Substantially Equivalent

Bovie Ultrasonic Surgical Aspirator

Mdt Corp., Inc., Salt Lake City UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932094 is the FDA 510(k) clearance record for BOVIE ULTRASONIC SURGICAL ASPIRATOR, cleared for Mdt Corp., Inc. on under FDA product code LFL (Instrument, Ultrasonic Surgical). FDA records list one 510(k) clearance for Mdt Corp., Inc. As of , FDA records show no recalls naming K932094.

Clearance record

Decision date
Received
(82 days to decision)
Product code
LFL Instrument, Ultrasonic Surgical
Device class
Unclassified
Review panel
Unknown
Applicant
Mdt Corp., Inc. 2471 E. Shadow Wood Cr., Salt Lake City UT
510(k) summary
Summary
Third party review
No

Clearances, product code LFL

Trailing 12 months
2 clearances under product code LFL in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LFL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20261