510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K790368Substantially Equivalent

Modified Thayer Martin Agar

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

K790368 is the FDA 510(k) clearance record for MODIFIED THAYER MARTIN AGAR, a class II device, cleared for Biomedia, Inc. on under FDA product code JTY (Culture Media, For Isolation Of Pathogenic Neisseria). FDA records list 19 510(k) clearances for Biomedia, Inc., from to . As of , FDA records show no recalls naming K790368.

Clearance record

Decision date
Received
(27 days to decision)
Product code
JTY Culture Media, For Isolation Of Pathogenic Neisseria
Regulation
21 CFR 866.2410
Device class
Class II
Review panel
Microbiology
Applicant
Biomedia, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JTY

Trailing 12 months

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

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