Cleared Traditional

K873994 - EASY-TEST ALBUMIN (ALB)

K873994 is the FDA 510(k) clearance for EASY-TEST ALBUMIN (ALB) by Em Diagnostic Systems, Inc.. It is a Class 2 Chemistry device (product code CIX) cleared through the Traditional 510(k) pathway after a 28-day FDA review.

K873994 · Em Diagnostic Systems, Inc. · Chemistry device
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Oct 1987
Decision
28d
Days
Class 2
Risk

K873994 is an FDA 510(k) clearance for the EASY-TEST ALBUMIN (ALB), ITEM NO. 19039. Classified as Bromcresol Green Dye-binding, Albumin (product code CIX), Class II - Special Controls.

Submitted by Em Diagnostic Systems, Inc. (Gibbstown, US). The FDA issued a Cleared decision on October 29, 1987 after a review of 28 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1035 - 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 Em Diagnostic Systems, Inc. devices

Submission Details

510(k) Number K873994 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 01, 1987
Decision Date October 29, 1987
Days to Decision 28 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
60d faster than avg
Panel avg: 88d · This submission: 28d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code CIX Bromcresol Green Dye-binding, Albumin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1035
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 - CIX Bromcresol Green Dye-binding, Albumin

All 76
Devices cleared under the same product code (CIX) and FDA review panel - the closest regulatory comparables to K873994.
WAKO(TM) AUTOKIT ALBUMIN
K880313 · Wako Chemicals USA, Inc. · Mar 1988
ALBUMIN, BROMCRESOL GREEN DYE-BINDING
K875070 · Tech-Co, Inc. · Jan 1988
ALBUMIN (BCG) FOR CONTINUOUS FLOW INSTRUMENTS
K874163 · Catachem, Inc. · Nov 1987
ALBUMIN REAGENT - BROMCRESOL GREEN METHOD
K870372 · Trace Scientific , Ltd. · Aug 1987
EASY-TEST ALBUMIN (ALB), ITEM NO. 67529/93
K864715 · Em Diagnostic Systems, Inc. · Dec 1986
ALBUMIN PROCEDURE
K863263 · Data Medical Associates, Inc. · Sep 1986