510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K791414Substantially Equivalent

Dtm (Dermatophyte Test Medium) Agar

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

K791414 is the FDA 510(k) clearance record for DTM (DERMATOPHYTE TEST MEDIUM) AGAR, a class I device, cleared for Biomedia, Inc. on under FDA product code JSI (Culture Media, Selective And Differential). FDA records list 19 510(k) clearances for Biomedia, Inc., from to . As of , FDA records show no recalls naming K791414.

Clearance record

Decision date
Received
(79 days to decision)
Product code
JSI Culture Media, Selective And Differential
Regulation
21 CFR 866.2360
Device class
Class I
Review panel
Microbiology
Applicant
Biomedia, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JSI

Trailing 12 months

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

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