510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K881539Substantially Equivalent

Amies Transport Medium

Neogen Culture Media, Baltimore MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K881539 is the FDA 510(k) clearance record for AMIES TRANSPORT MEDIUM, a class I device, cleared for Acumedia Manufacturers, Inc. on under FDA product code JSM (Culture Media, Non-Propagating Transport). FDA records list 177 510(k) clearances for Neogen Culture Media, from to . As of , FDA records show no recalls naming K881539.

Clearance record

Decision date
Received
(10 days to decision)
Product code
JSM Culture Media, Non-Propagating Transport
Regulation
21 CFR 866.2390
Device class
Class I
Review panel
Microbiology
Applicant
Acumedia Manufacturers, Inc. 3651 Clipper Mill Rd., Baltimore MD
Third party review
No

Clearances, product code JSM

Trailing 12 months
1 clearance under product code JSM in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JSM, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260