Cleared Traditional

K864239 - CLED AGAR WITH ANDRADES INDICATOR

K864239 is the FDA 510(k) clearance for CLED AGAR WITH ANDRADES INDICATOR by Mds Laboratories, Inc.. It is a Class 1 Microbiology device (product code JSH) cleared through the Traditional 510(k) pathway after a 154-day FDA review.

K864239 · Mds Laboratories, Inc. · Microbiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1987
Decision
154d
Days
Class 1
Risk

K864239 is an FDA 510(k) clearance for the CLED AGAR WITH ANDRADES INDICATOR. Classified as Culture Media, Non-selective And Differential (product code JSH), Class I - General Controls.

Submitted by Mds Laboratories, Inc. (L5j 2m4, CA). The FDA issued a Cleared decision on March 31, 1987 after a review of 154 days - an extended review cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2320 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Microbiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Mds Laboratories, Inc. devices

Submission Details

510(k) Number K864239 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 28, 1986
Decision Date March 31, 1987
Days to Decision 154 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
52d slower than avg
Panel avg: 102d · This submission: 154d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JSH Culture Media, Non-selective And Differential
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2320
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 - JSH Culture Media, Non-selective And Differential

All 102
Devices cleared under the same product code (JSH) and FDA review panel - the closest regulatory comparables to K864239.
HEMOPHILUS ID QUAD PLATE
K870636 · Hardy Media · Apr 1987
BIGGY AGAR
K870651 · Hardy Media · Apr 1987
CLED AGAR
K871095 · bioMerieux, Inc. · Apr 1987
THERMONUCLEASE AGAR W/TOLUIDINE BLUE
K864205 · Remel Co. · Nov 1986
TRYCOPHYTON AGARS
K864100 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Oct 1986
XANTHINE/TYROSINE/CASEIN AGAR
K863572 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Sep 1986