510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K883522Substantially Equivalent

Amerimed Ultrasonic Surgical Aspiration Kit

Amerimed US Corp., Denver CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K883522 is the FDA 510(k) clearance record for AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT, cleared for Amerimed US Corp. on under FDA product code LBK (Neurosurgical Ultrasonic Instruments). FDA records list 5 510(k) clearances for Amerimed US Corp., from to . As of , FDA records show no recalls naming K883522.

Clearance record

Decision date
Received
(44 days to decision)
Product code
LBK Neurosurgical Ultrasonic Instruments
Device class
Unclassified
Review panel
Unknown
Applicant
Amerimed US Corp. 777 Grant, Suite 305, Denver CO
Third party review
No

Clearances, product code LBK

Trailing 12 months

FDA records hold no clearances under product code LBK in the trailing twelve months.

FDA records show no clearances under product code LBK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LBK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260