510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K811513Substantially Equivalent

Wilkins-Chalgren Anaerobe Agar

Oxoid U.S.A., Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K811513 is the FDA 510(k) clearance record for WILKINS-CHALGREN ANAEROBE AGAR, a class II device, cleared for Oxoid U.S.A., Inc. on under FDA product code JSO (Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar). FDA records list 93 510(k) clearances for Oxoid U.S.A., Inc., from to . As of , FDA records show no recalls naming K811513.

Clearance record

Decision date
Received
(21 days to decision)
Product code
JSO Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar
Regulation
21 CFR 866.1700
Device class
Class II
Review panel
Microbiology
Applicant
Oxoid U.S.A., Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JSO

Trailing 12 months

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

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