Cleared Traditional

K885282 - ASSAYED CHOLINESTERASE CONTROL

K885282 is an FDA 510(k) clearance for ASSAYED CHOLINESTERASE CONTROL, manufactured by Actio, Inc.. The device is a Class 1 Chemistry device with product code JJX cleared through the Traditional 510(k) pathway after a 171-day FDA review.

K885282 · Actio, Inc. · Chemistry device
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Jun 1989
Decision
171d
Days
Class 1
Risk

K885282 is an FDA 510(k) clearance for the ASSAYED CHOLINESTERASE CONTROL. Classified as Single (specified) Analyte Controls (assayed And Unassayed) (product code JJX), Class I - General Controls.

Submitted by Actio, Inc. (Oakland, US). The FDA issued a Cleared decision on June 9, 1989 after a review of 171 days - an extended review cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1660 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Chemistry review framework, consistent with the majority of Class II 510(k) submissions.

View all Actio, Inc. devices

FDA 510(k) Submission Details - K885282

510(k) Number K885282 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 20, 1988
Decision Date June 09, 1989
Days to Decision 171 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
83d slower than avg
Panel avg: 88d · This submission: 171d
Pathway characteristics
Predicate-based equivalence.

JJX Device Classification - Class 1, General Controls

Product Code JJX Single (specified) Analyte Controls (assayed And Unassayed)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1660
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 - JJX Single (specified) Analyte Controls (assayed And Unassayed)

All 461
Devices cleared under the same product code (JJX) and FDA review panel - the closest regulatory comparables to K885282.
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