Cleared Traditional

K834125 - CHLAMYDIAL TRANSPORT MEDIUM

K834125 is the FDA 510(k) clearance for CHLAMYDIAL TRANSPORT MEDIUM by Bartels Immunodiagnostic Supplies, Inc.. It is a Class 1 Microbiology device (product code JSM) cleared through the Traditional 510(k) pathway after a 76-day FDA review.

K834125 · Bartels Immunodiagnostic Supplies, Inc. · Microbiology device
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Feb 1984
Decision
76d
Days
Class 1
Risk

K834125 is an FDA 510(k) clearance for the CHLAMYDIAL TRANSPORT MEDIUM. Classified as Culture Media, Non-propagating Transport (product code JSM), Class I - General Controls.

Submitted by Bartels Immunodiagnostic Supplies, Inc. (Mchenry, US). The FDA issued a Cleared decision on February 13, 1984 after a review of 76 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2390 - 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 Bartels Immunodiagnostic Supplies, Inc. devices

Submission Details

510(k) Number K834125 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 29, 1983
Decision Date February 13, 1984
Days to Decision 76 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
26d faster than avg
Panel avg: 102d · This submission: 76d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JSM Culture Media, Non-propagating Transport
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2390
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 - JSM Culture Media, Non-propagating Transport

All 49
Devices cleared under the same product code (JSM) and FDA review panel - the closest regulatory comparables to K834125.
BBL PORT-A-CUL AEROBIC TRANSPORT SYS, MODIFIED STU
K854986 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Jan 1986
SYVA MYCOTRANS MYCOPLASMA TRANSPORT SYSTEM
K854061 · Syva Co. · Oct 1985
ORTHO VIRAL TRANSPORT
K853500 · Ortho Diagnostic Systems, Inc. · Aug 1985
STERILE SALINE 0.85%
K834315 · Hardy Media · Jan 1984
WATER W/TWEEN 80
K834316 · Hardy Media · Jan 1984
VIRAL TRANSPORT MED. (46-995-04)
K802303 · Flow Laboratories, Inc. · Oct 1980