Cleared Traditional

K860350 - SERUM CHOLINESTERASE REAGENT SET

K860350 is the FDA 510(k) clearance for SERUM CHOLINESTERASE REAGENT SET by Sterling Diagnostics, Inc.. It is a Class 1 Chemistry device (product code DLI) cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K860350 · Sterling Diagnostics, Inc. · Chemistry device
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Apr 1986
Decision
84d
Days
Class 1
Risk

K860350 is an FDA 510(k) clearance for the SERUM CHOLINESTERASE REAGENT SET. Classified as Acetylcholine Chloride, Specific Reagent For Pseudo Cholinesterase (product code DLI), Class I - General Controls.

Submitted by Sterling Diagnostics, Inc. (Sterling Heights, US). The FDA issued a Cleared decision on April 24, 1986 after a review of 84 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.3240 - 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 Sterling Diagnostics, Inc. devices

Submission Details

510(k) Number K860350 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 30, 1986
Decision Date April 24, 1986
Days to Decision 84 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
4d faster than avg
Panel avg: 88d · This submission: 84d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code DLI Acetylcholine Chloride, Specific Reagent For Pseudo Cholinesterase
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.3240
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 - DLI Acetylcholine Chloride, Specific Reagent For Pseudo Cholinesterase

Devices cleared under the same product code (DLI) and FDA review panel - the closest regulatory comparables to K860350.
DUPONT DIMENSION(R) PSEUDOCHOLINESTERASE METHOD
K950180 · E.I. Dupont DE Nemours & Co., Inc. · Mar 1995
CHOLINESTERASE METHOD FOR TECHNICON CHEM1/TECHNICO
K930208 · Heraeus Kulzer, Inc. · Apr 1993
EASY-TEST (CHE) REAGENT, ITEM NO. 67522/93
K860641 · Em Diagnostic Systems, Inc. · Apr 1986
CHOLINESTERASE REAGENT SYSTEM
K771024 · American Monitor Corp. · Jul 1977