510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K092330Substantially Equivalent

Oc-Sensor Diana Ifob Test

Polymedco Cancer Diagnostics, LLC, Cortlandt Manor NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K092330 is the FDA 510(k) clearance record for OC-SENSOR DIANA IFOB TEST, a class II device, cleared for Polymedco Cancer Diagnostics, LLC on under FDA product code OOX (Automated Occult Blood Analyzer). FDA's definition for product code OOX reads: "The automated test system is intended for the qualitative detection of fecal occult blood in feces by professional laboratories. The automated test is used for the determination of gastrointestinal bleeding". FDA records list one 510(k) clearance for Polymedco Cancer Diagnostics, LLC. As of , FDA records show no recalls naming K092330.

Clearance record

Decision date
Received
(157 days to decision)
Product code
OOX Automated Occult Blood Analyzer
Regulation
21 CFR 864.6550
Device class
Class II
Review panel
Hematology
Applicant
Polymedco Cancer Diagnostics, LLC 510 Furnace Dock Rd., Cortlandt Manor NY
510(k) summary
Statement
Third party review
Yes

Clearances, product code OOX

Trailing 12 months

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

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