Cleared Traditional

K884269 - SAMPLE IDENTIFICATION STATION MODEL 38010

K884269 is an FDA 510(k) clearance for SAMPLE IDENTIFICATION STATION MODEL 38010, manufactured by Icn Micromedic Systems. The device is a Class 1 Chemistry device with product code JJJ cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K884269 · Icn Micromedic Systems · Chemistry device
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Jan 1989
Decision
90d
Days
Class 1
Risk

K884269 is an FDA 510(k) clearance for the SAMPLE IDENTIFICATION STATION MODEL 38010. Classified as Counter (beta, Gamma) For Clinical Use (product code JJJ), Class I - General Controls.

Submitted by Icn Micromedic Systems (Horsham, US). The FDA issued a Cleared decision on January 9, 1989 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.2320 - 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 Icn Micromedic Systems devices

FDA 510(k) Submission Details - K884269

510(k) Number K884269 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 11, 1988
Decision Date January 09, 1989
Days to Decision 90 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
2d slower than avg
Panel avg: 88d · This submission: 90d
Pathway characteristics
Predicate-based equivalence.

JJJ Device Classification - Class 1, General Controls

Product Code JJJ Counter (beta, Gamma) For Clinical Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.2320
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 - JJJ Counter (beta, Gamma) For Clinical Use

All 33
Devices cleared under the same product code (JJJ) and FDA review panel - the closest regulatory comparables to K884269.
SEQUENTIAL SAMPLE MULTI-PHOTON DETECTOR
K962762 · Biotraces, Inc. · Aug 1996
ABBOTT VERTEX ANALYZER
K920559 · Abbott Laboratories · Mar 1992
1205 BETAPLATE LIQUID SCINTILLATION COUNTER
K874094 · Lkb Instruments, Inc. · Nov 1987
TAURUS (TM) AUTOMATIC LIQUID SCINTILLATION COUNTER
K862206 · Micromedic Systems · Aug 1986
DENTOCULT CULTURE-PADDLE
K851164 · Orion Corp. · Oct 1985
1208 BETACORD AND 1208 BETCORD M
K852434 · Lkb Instruments, Inc. · Aug 1985