510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K911419Substantially Equivalent

Sensititre Aris Module

Sensititre, Ltd., Westlake OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K911419 is the FDA 510(k) clearance record for SENSITITRE ARIS MODULE, a class II device, cleared for Sensititre , Ltd. on under FDA product code LRG (Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems). FDA records list 3 510(k) clearances for Sensititre , Ltd., from to . As of , FDA records show no recalls naming K911419.

Clearance record

Decision date
Received
(457 days to decision)
Product code
LRG Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems
Regulation
21 CFR 866.1640
Device class
Class II
Review panel
Microbiology
Applicant
Sensititre , Ltd. 811 Sharon Dr., Westlake OH
Third party review
No

Clearances, product code LRG

Trailing 12 months

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

FDA records show no clearances under product code LRG in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LRG, 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