Cleared Traditional

K863265 - DIRECT BILIRUBIN PROCEDURE

K863265 is the FDA 510(k) clearance for DIRECT BILIRUBIN PROCEDURE by Data Medical Associates, Inc.. It is a Class 2 Toxicology device (product code CIG) cleared through the Traditional 510(k) pathway after a 60-day FDA review.

K863265 · Data Medical Associates, Inc. · Toxicology device
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Oct 1986
Decision
60d
Days
Class 2
Risk

K863265 is an FDA 510(k) clearance for the DIRECT BILIRUBIN PROCEDURE. Classified as Diazo Colorimetry, Bilirubin (product code CIG), Class II - Special Controls.

Submitted by Data Medical Associates, Inc. (Arlington, US). The FDA issued a Cleared decision on October 24, 1986 after a review of 60 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.1110 - 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 Data Medical Associates, Inc. devices

Submission Details

510(k) Number K863265 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 25, 1986
Decision Date October 24, 1986
Days to Decision 60 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
27d faster than avg
Panel avg: 87d · This submission: 60d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code CIG Diazo Colorimetry, Bilirubin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1110
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 - CIG Diazo Colorimetry, Bilirubin

All 171
Devices cleared under the same product code (CIG) and FDA review panel - the closest regulatory comparables to K863265.
REAGENTS 1263,1273,1284,1425,014301,053583
K871531 · American Research Products Co. · May 1987
TOTAL BILIRUBIN REAGENT 1372,1425,1284,1273,053583
K871530 · American Research Products Co. · May 1987
BILIRUBIN TOTAL
K863056 · J. D. Assoc. · Nov 1986
BILIRUBIN TOTAL DIRECT
K863057 · J. D. Assoc. · Sep 1986
TOTAL BILIRUBIN PROCEDURE
K863262 · Data Medical Associates, Inc. · Sep 1986
BILIFAST
K863055 · J. D. Assoc. · Sep 1986