510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K121991Substantially Equivalent

Enterococcus Quickfish Bc

Advandx, Inc., Woburn MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K121991 is the FDA 510(k) clearance record for ENTEROCOCCUS QUICKFISH BC, a class I device, cleared for Advandx, Inc. on under FDA product code OAH (Fish (Fluorescent In Situ Hybridization) Kit, Protein Nucleic Acid, Enterococcus Faecalis). FDA's definition for product code OAH reads: "E. Faecalis pna fish is a qualitative nucleic acid hybridization assay intended for the identification of enterococcus faecalis and other enterococci (oe) from blood cultures showing Gram-positive cocci in pairs and chains". FDA records list 21 510(k) clearances for Advandx, Inc., from to . As of , FDA records show no recalls naming K121991.

Clearance record

Decision date
Received
(185 days to decision)
Product code
OAH Fish (Fluorescent In Situ Hybridization) Kit, Protein Nucleic Acid, Enterococcus Faecalis
Regulation
21 CFR 866.3740
Device class
Class I
Review panel
Microbiology
Applicant
Advandx, Inc. 400 Tradecenter Suite 6990, Woburn MA
510(k) summary
Statement
Third party review
No

Clearances, product code OAH

Trailing 12 months

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

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