510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K962574Substantially Equivalent

Waters 474 Scanning Flourescence Detector (474)

Waters Corporation, Milford MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K962574 is the FDA 510(k) clearance record for WATERS 474 SCANNING FLOURESCENCE DETECTOR (474), a class I device, cleared for Waters Corporation on under FDA product code LEQ (Detectors, Electrochemical, Liquid Chromatography). FDA records list 6 510(k) clearances for Waters Corporation, from to . As of , FDA records show no recalls naming K962574.

Clearance record

Decision date
Received
(21 days to decision)
Product code
LEQ Detectors, Electrochemical, Liquid Chromatography
Regulation
21 CFR 862.2260
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Waters Corporation 34 Maple St., Milford MA
510(k) summary
Statement
Third party review
No

Clearances, product code LEQ

Trailing 12 months

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

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