Cleared Traditional

K861974 - PERCEPTIVE SYSTEMS INC PSICOM 217 KARYOTYPING SYST

K861974 is an FDA 510(k) clearance for PERCEPTIVE SYSTEMS INC PSICOM 217 KARYO..., manufactured by Perceptive Systems, Inc.. The device is a Class 2 Pathology device with product code LNJ cleared through the Traditional 510(k) pathway after a 75-day FDA review.

K861974 · Perceptive Systems, Inc. · Pathology device
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Aug 1986
Decision
75d
Days
Class 2
Risk

K861974 is an FDA 510(k) clearance for the PERCEPTIVE SYSTEMS INC PSICOM 217 KARYOTYPING SYST. Classified as Analyzer, Chromosome, Automated (product code LNJ), Class II - Special Controls.

Submitted by Perceptive Systems, Inc. (Houston, US). The FDA issued a Cleared decision on August 4, 1986 after a review of 75 days - a notably fast clearance cycle.

This device falls under the Pathology FDA review panel, regulated under 21 CFR 864.5260 - the FDA pathology device 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 Perceptive Systems, Inc. devices

FDA 510(k) Submission Details - K861974

510(k) Number K861974 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 21, 1986
Decision Date August 04, 1986
Days to Decision 75 days
Submission Type Traditional
Review Panel Pathology (PA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
3d faster than avg
Panel avg: 78d · This submission: 75d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LNJ Device Classification - Class 2, Special Controls

Product Code LNJ Analyzer, Chromosome, Automated
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.5260
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 Pathology devices follow this clearance model.