510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K923892Substantially Equivalent

Smith River Microbiological Culture Media

Smith River Biologicals, Ferrum VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923892 is the FDA 510(k) clearance record for SMITH RIVER MICROBIOLOGICAL CULTURE MEDIA, a class II device, cleared for Smith River Biologicals on under FDA product code JSO (Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar). FDA records list 12 510(k) clearances for Smith River Biologicals, from to . As of , FDA records show no recalls naming K923892.

Clearance record

Decision date
Received
(321 days to decision)
Product code
JSO Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar
Regulation
21 CFR 866.1700
Device class
Class II
Review panel
Microbiology
Applicant
Smith River Biologicals Rt. 3, Ferrum VA
510(k) summary
Statement
Third party review
No

Clearances, product code JSO

Trailing 12 months

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

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