510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K831918Substantially Equivalent

La-Staph Identification System

IMMY, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K831918 is the FDA 510(k) clearance record for LA-STAPH IDENTIFICATION SYSTEM, a class I device, cleared for Immuno-Mycologics, Inc. on under FDA product code JWX (Kit, Screening, Staphylococcus Aureus). FDA records list 26 510(k) clearances for IMMY, Inc., from to . As of , FDA records show no recalls naming K831918.

Clearance record

Decision date
Received
(0 days to decision)
Product code
JWX Kit, Screening, Staphylococcus Aureus
Regulation
21 CFR 866.2660
Device class
Class I
Review panel
Microbiology
Applicant
Immuno-Mycologics, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JWX

Trailing 12 months

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

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