Cleared Traditional

K875069 - BILIRUBIN (TOTAL)

K875069 is the FDA 510(k) clearance for BILIRUBIN (TOTAL) by Tech-Co, Inc.. It is a Class 2 Chemistry device (product code CIG) cleared through the Traditional 510(k) pathway after a 33-day FDA review.

K875069 · Tech-Co, Inc. · Chemistry device
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Jan 1988
Decision
33d
Days
Class 2
Risk

K875069 is an FDA 510(k) clearance for the BILIRUBIN (TOTAL). Classified as Diazo Colorimetry, Bilirubin (product code CIG), Class II - Special Controls.

Submitted by Tech-Co, Inc. (Oak Park, US). The FDA issued a Cleared decision on January 11, 1988 after a review of 33 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1110 - the FDA in vitro diagnostics and chemistry 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 Tech-Co, Inc. devices

Submission Details

510(k) Number K875069 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 09, 1987
Decision Date January 11, 1988
Days to Decision 33 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
55d faster than avg
Panel avg: 88d · This submission: 33d
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 Chemistry devices follow this clearance model.

Regulatory Peers - CIG Diazo Colorimetry, Bilirubin

All 175
Devices cleared under the same product code (CIG) and FDA review panel - the closest regulatory comparables to K875069.
TOTAL BILIRUBIN PROCEDURE RUN ON A DEMAND INSTRU.
K880395 · Data Medical Associates, Inc. · Mar 1988
TOTAL BILIRUBIN PROCEDURE RUN ON A AU5000 INSTRU.
K880396 · Data Medical Associates, Inc. · Mar 1988
DIRECT BILIRUBIN PROCEDURE RUN ON A AU5000 INSTRU.
K880397 · Data Medical Associates, Inc. · Mar 1988
IQ/QCA TOTAL BILIRUBIN
K874261 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Nov 1987
REFLOTRON BILIRUBIN
K872818 · Boehringer Mannheim Corp. · Nov 1987
CONJUGATED BILIRUBIN (CBIL) ITEM NO. 67684/95
K873551 · Em Diagnostic Systems, Inc. · Oct 1987