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
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K210511Substantially Equivalent

InTray GC

Biomed Diagnostics Incorporated, White City OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K210511 is the FDA 510(k) clearance record for InTray GC, a class II device, cleared for Biomed Diagnostics Incorporated on under FDA product code JTY (Culture Media, For Isolation Of Pathogenic Neisseria). FDA records list one 510(k) clearance for Biomed Diagnostics Incorporated. As of , FDA records show no recalls naming K210511.

Clearance record

Decision date
Received
(239 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
Biomed Diagnostics Incorporated 1388 Antelope Rd., White City OR
510(k) summary
Summary PDF
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