Cleared Traditional

K973074 - 2487 DUAL WAVELENGTH ABSORBANCE DETECTOR

K973074 is the FDA 510(k) clearance for 2487 DUAL WAVELENGTH ABSORBANCE DETECTOR by Waters Corporation. It is a Class 1 Toxicology device (product code KZR) cleared through the Traditional 510(k) pathway after a 49-day FDA review.

K973074 · Waters Corporation · Toxicology device
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Oct 1997
Decision
49d
Days
Class 1
Risk

K973074 is an FDA 510(k) clearance for the 2487 DUAL WAVELENGTH ABSORBANCE DETECTOR. Classified as Chromatography (liquid, Gel), Clinical Use (product code KZR), Class I - General Controls.

Submitted by Waters Corporation (Milford, US). The FDA issued a Cleared decision on October 6, 1997 after a review of 49 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.2260 - the FDA toxicology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Waters Corporation devices

Submission Details

510(k) Number K973074 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 18, 1997
Decision Date October 06, 1997
Days to Decision 49 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
38d faster than avg
Panel avg: 87d · This submission: 49d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KZR Chromatography (liquid, Gel), Clinical Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.2260
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - KZR Chromatography (liquid, Gel), Clinical Use

All 11
Devices cleared under the same product code (KZR) and FDA review panel - the closest regulatory comparables to K973074.
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