510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K002165Substantially Equivalent

Linezolid, 30Ug, Bbl Sensi-Disc

Dickinson, and Co., Sparks MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K002165 is the FDA 510(k) clearance record for LINEZOLID, 30UG, BBL SENSI-DISC, a class II device, cleared for Dickinson, and Co. on under FDA product code JTN (Susceptibility Test Discs, Antimicrobial). FDA records list one 510(k) clearance for Dickinson, and Co. As of , FDA records show no recalls naming K002165.

Clearance record

Decision date
Received
(49 days to decision)
Product code
JTN Susceptibility Test Discs, Antimicrobial
Regulation
21 CFR 866.1620
Device class
Class II
Review panel
Microbiology
Applicant
Dickinson, and Co. 7loveton Cir., Sparks MD
510(k) summary
Summary
Third party review
No

Clearances, product code JTN

Trailing 12 months
6 clearances under product code JTN in the twelve months to October 2026, July 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code JTN, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20262
August 20261
September 20260
October 20260