510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K881575Substantially Equivalent

Selective Streptococcus Agar

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

K881575 is the FDA 510(k) clearance record for SELECTIVE STREPTOCOCCUS AGAR, a class I device, cleared for Acumedia Manufacturers, Inc. on under FDA product code JSI (Culture Media, Selective And Differential). FDA records list 177 510(k) clearances for Neogen Culture Media, from to . As of , FDA records show no recalls naming K881575.

Clearance record

Decision date
Received
(7 days to decision)
Product code
JSI Culture Media, Selective And Differential
Regulation
21 CFR 866.2360
Device class
Class I
Review panel
Microbiology
Applicant
Acumedia Manufacturers, Inc. 3651 Clipper Mill Rd., Baltimore MD
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