Cleared Traditional

K881649 - MODIFIED PARACON(TM) CONCENTRATION KIT

K881649 is an FDA 510(k) clearance for MODIFIED PARACON(TM) CONCENTRATION KIT, manufactured by Para Scientific Co.. The device is a Class 1 Microbiology device with product code LKS cleared through the Traditional 510(k) pathway after a 6-day FDA review.

K881649 · Para Scientific Co. · Microbiology device
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Apr 1988
Decision
6d
Days
Class 1
Risk

K881649 is an FDA 510(k) clearance for the MODIFIED PARACON(TM) CONCENTRATION KIT. Classified as Device, Parasite Concentration (product code LKS), Class I - General Controls.

Submitted by Para Scientific Co. (Lake Oswego, US). The FDA issued a Cleared decision on April 21, 1988 after a review of 6 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2900 - the FDA microbiology 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.

FDA 510(k) Submission Details - K881649

510(k) Number K881649 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 15, 1988
Decision Date April 21, 1988
Days to Decision 6 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
96d faster than avg
Panel avg: 102d · This submission: 6d
Pathway characteristics
Predicate-based equivalence.

LKS Device Classification - Class 1, General Controls

Product Code LKS Device, Parasite Concentration
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2900
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 - LKS Device, Parasite Concentration

All 12
Devices cleared under the same product code (LKS) and FDA review panel - the closest regulatory comparables to K881649.
STOOL TRANSPORT/PROCESSOR
K933370 · Sage Products, Inc. · Feb 1994
PARASAFE(R) FIXATIVE
K935316 · Scientific Device Laboratory, Inc. · Feb 1994
PARAPREP
K931849 · Medastat Scientific Corp. · Dec 1993
PARA-PAK MACRO-CON
K860034 · Meridian Diagnostics, Inc. · Feb 1986
PARA CON TM
K853715 · Para Scientific Co. · Oct 1985
FPC FECAL PARASITE CONCENTRATOR
K833469 · Evergreen Scientific, Inc. · Nov 1983
K881649 · MODIFIED PARACON(TM) CONCENTRATION KIT
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