Cleared Traditional

K871278 - MODIFIED CHLAMYDIA DIRECT SPECIMEN TEST KIT

K871278 is an FDA 510(k) clearance for MODIFIED CHLAMYDIA DIRECT SPECIMEN TEST KIT, manufactured by California Integrated Diagnostics, Inc.. The device is a Class 1 Microbiology device with product code LJP cleared through the Traditional 510(k) pathway after a 8-day FDA review.

K871278 · California Integrated Diagnostics, Inc. · Microbiology device
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Apr 1987
Decision
8d
Days
Class 1
Risk

K871278 is an FDA 510(k) clearance for the MODIFIED CHLAMYDIA DIRECT SPECIMEN TEST KIT. Classified as Antiserum, Fluorescent, Chlamydia Trachomatis (product code LJP), Class I - General Controls.

Submitted by California Integrated Diagnostics, Inc. (Berkeley, US). The FDA issued a Cleared decision on April 8, 1987 after a review of 8 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.3120 - 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.

View all California Integrated Diagnostics, Inc. devices

FDA 510(k) Submission Details - K871278

510(k) Number K871278 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 31, 1987
Decision Date April 08, 1987
Days to Decision 8 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
94d faster than avg
Panel avg: 102d · This submission: 8d
Pathway characteristics
Predicate-based equivalence.

LJP Device Classification - Class 1, General Controls

Product Code LJP Antiserum, Fluorescent, Chlamydia Trachomatis
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.3120
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 - LJP Antiserum, Fluorescent, Chlamydia Trachomatis

All 31
Devices cleared under the same product code (LJP) and FDA review panel - the closest regulatory comparables to K871278.
MICROTRAK CHLAMYDIA TRACHO. TEST - METHANOL FIXAT.
K872903 · Syva Co. · Aug 1987
CHLAMYDIA-CHECK(TM) DIRECT & CULTURE CONFIR. KIT
K864128 · Diagnostic Technology, Inc. · Apr 1987
MONABRITE CHLAMYDIA TRACHOMATIS DIR. SPECIMEN TEST
K870946 · Serono Diagnostics, Inc. · Apr 1987
CHLAMYDIAE FLUOR. AB TEST FOR DETECTION IN SMEARS
K864662 · American Micro Scan · Mar 1987
MODIFIED IMAGEN(TM) CHLAMYDIA TEST
K864539 · Boots-Celltech Diagnostics, Inc. · Mar 1987
MICROTRAK CHLAMYDIA TRACHOMATIS DIRECT SPECI. TEST
K864888 · Syva Co. · Feb 1987