510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K852539Substantially Equivalent

Suszoi Ultrasonic Surgical Aspirator Sonop

Johnson & Johnson Professionals, Inc., Ramsey NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K852539 is the FDA 510(k) clearance record for SUSZOI ULTRASONIC SURGICAL ASPIRATOR SONOP, cleared for Johnson & Johnson Professionals, Inc. on under FDA product code LFL (Instrument, Ultrasonic Surgical). FDA records list 206 510(k) clearances for Johnson & Johnson Professionals, Inc., from to . As of , FDA records show no recalls naming K852539.

Clearance record

Decision date
Received
(39 days to decision)
Product code
LFL Instrument, Ultrasonic Surgical
Device class
Unclassified
Review panel
Unknown
Applicant
Johnson & Johnson Professionals, Inc. 69 Spring St., Ramsey NJ
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