Cleared Traditional

K850457 - DU PONT DIGOXIN ASSAY CALIBRATOR

K850457 is the FDA 510(k) clearance for DU PONT DIGOXIN ASSAY CALIBRATOR by E.I. Dupont DE Nemours & Co., Inc.. It is a Class 2 Toxicology device (product code DLJ) cleared through the Traditional 510(k) pathway after a 27-day FDA review.

K850457 · E.I. Dupont DE Nemours & Co., Inc. · Toxicology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1985
Decision
27d
Days
Class 2
Risk

K850457 is an FDA 510(k) clearance for the DU PONT DIGOXIN ASSAY CALIBRATOR. Classified as Calibrators, Drug Specific (product code DLJ), Class II - Special Controls.

Submitted by E.I. Dupont DE Nemours & Co., Inc. (Wilmington, US). The FDA issued a Cleared decision on March 5, 1985 after a review of 27 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3200 - 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 E.I. Dupont DE Nemours & Co., Inc. devices

Submission Details

510(k) Number K850457 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 06, 1985
Decision Date March 05, 1985
Days to Decision 27 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
60d faster than avg
Panel avg: 87d · This submission: 27d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DLJ Calibrators, Drug Specific
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3200
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Toxicology devices follow this clearance model.

Regulatory Peers - DLJ Calibrators, Drug Specific

All 93
Devices cleared under the same product code (DLJ) and FDA review panel - the closest regulatory comparables to K850457.
EMIT QUINIDINE CALIBRATOR ITEM NO. 67631/93
K870247 · Em Diagnostic Systems, Inc. · Feb 1987
ANTIASTHMATIC CALIBRATORS
K862964 · American Monitor Corp. · Aug 1986
EMIT COLUMN DIGOXIN CALIBRATORS
K861395 · Syva Co. · May 1986
DU PONT TOBRAMYCIN ASSAY CALIBRATOR
K850057 · E.I. Dupont DE Nemours & Co., Inc. · Jan 1985
DU PONT GENTAMICIN ASSAY CALIBRATOR
K850059 · E.I. Dupont DE Nemours & Co., Inc. · Jan 1985
EMIT 700 CANNABINOID CALIBRATOR
K843420 · Syva Co. · Sep 1984