Cleared Traditional

K892213 - ACS COLLOID OSMOTIC PRESSURE CALIBRATOR

K892213 is the FDA 510(k) clearance for ACS COLLOID OSMOTIC PRESSURE CALIBRATOR by Analytical Control Systems, Inc.. It is a Class 2 Chemistry device (product code JIW) cleared through the Traditional 510(k) pathway after a 79-day FDA review.

K892213 · Analytical Control Systems, Inc. · Chemistry device
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Jun 1989
Decision
79d
Days
Class 2
Risk

K892213 is an FDA 510(k) clearance for the ACS COLLOID OSMOTIC PRESSURE CALIBRATOR. Classified as Calibrator, Surrogate (product code JIW), Class II - Special Controls.

Submitted by Analytical Control Systems, Inc. (Fishers, US). The FDA issued a Cleared decision on June 21, 1989 after a review of 79 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1150 - 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 Analytical Control Systems, Inc. devices

Submission Details

510(k) Number K892213 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 03, 1989
Decision Date June 21, 1989
Days to Decision 79 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
9d faster than avg
Panel avg: 88d · This submission: 79d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JIW Calibrator, Surrogate
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1150
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 - JIW Calibrator, Surrogate

All 12
Devices cleared under the same product code (JIW) and FDA review panel - the closest regulatory comparables to K892213.
FLOW CYTOMETRY FITC/PE COMPENSATION KIT
K910255 · Sigma Diagnostics, Inc. · Apr 1991
SOPHEIA 1000 (S1CAL) & SOPHEIA 2000 (S2CAL)
K902575 · Diagnostic Products Corp. · Oct 1990
ACCUSCAN MICROBEAD STANDARDS
K902294 · Sigma Chemical Co. · Jul 1990
RAICHEM(TM) BILIRUBIN CONJUGATE STANDARD
K883389 · Reagents Applications, Inc. · Dec 1988
CALIBRATION KIT
K882220 · King Diagnostics, Inc. · Aug 1988
AMRESCO LIQUIZYME GLUCOSE/BUN STANDARD 0124, 0200
K880654 · American Research Products Co. · Jun 1988