510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K890339Substantially Equivalent

Difco Director Inoculation System

Difco Laboratories, Inc., Detroit MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K890339 is the FDA 510(k) clearance record for DIFCO DIRECTOR INOCULATION SYSTEM, a class II device, cleared for Difco Laboratories, Inc. on under FDA product code LIE (Reagent/Device, Inoculum Calibration). FDA records list 121 510(k) clearances for Difco Laboratories, Inc., from to . As of , FDA records show no recalls naming K890339.

Clearance record

Decision date
Received
(15 days to decision)
Product code
LIE Reagent/Device, Inoculum Calibration
Regulation
21 CFR 866.1640
Device class
Class II
Review panel
Microbiology
Applicant
Difco Laboratories, Inc. P. O. Box 331058, Detroit MI
Third party review
No

Clearances, product code LIE

Trailing 12 months

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

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