Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K923349Substantially Equivalent

Fungi Fluor Kit

Polysciences, Inc., Warrington PA / Traditional, Substantially Equivalent

K923349 is the FDA 510(k) clearance record for FUNGI FLUOR KIT, a class II device, cleared for Polysciences, Inc. on under FDA product code LYF (Pneumocystis Carinii). FDA records list 3 510(k) clearances for Polysciences, Inc., from to . As of , FDA records show no recalls naming K923349.

Clearance record

Decision date
Received
(104 days to decision)
Product code
LYF Pneumocystis Carinii
Regulation
21 CFR 866.3780
Device class
Class II
Review panel
Microbiology
Applicant
Polysciences, Inc. 400 Valley Rd., Warrington PA
510(k) summary
Summary
Third party review
No

Clearances, product code LYF

Trailing 12 months

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

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