Cleared Traditional

S S AGAR PLATE (K834423) - FDA 510(k) Clearance

Class I Microbiology device.

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Oct 1984
Decision
313d
Days
Class 1
Risk

K834423 is an FDA 510(k) clearance for the S S AGAR PLATE. Classified as Culture Media, Selective And Differential (product code JSI), Class I - General Controls.

Submitted by Otisville Biotech, Inc. (Walker, US). The FDA issued a Cleared decision on October 23, 1984 after a review of 313 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2360 - 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. Elevated predicate reliance profile. 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 Otisville Biotech, Inc. devices

Submission Details

510(k) Number K834423 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 15, 1983
Decision Date October 23, 1984
Days to Decision 313 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
211d slower than avg
Panel avg: 102d · This submission: 313d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JSI Culture Media, Selective And Differential
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2360
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 - JSI Culture Media, Selective And Differential

All 284
Devices cleared under the same product code (JSI) and FDA review panel - the closest regulatory comparables to K834423.
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ANAEROBIC LKV BLOOD AGAR
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BRILLIANT GREEN AGAR
K871094 · bioMerieux, Inc. · Apr 1987
CANDIDA BROM CRESOL GREEN AGAR
K864077 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Oct 1986
CAL (CELLOBIOSE-ARGININE-LYSINE) AGAR
K863519 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Sep 1986
DERMATOPHYTE TEST MEDIUM, SLANTS AND MYCOFLASKS
K863525 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Sep 1986