Cleared Traditional

K811514 - BACILLUS CEREUS SELECTIVE(AGAR&SUPP)

K811514 is the FDA 510(k) clearance for BACILLUS CEREUS SELECTIVE(AGAR&SUPP) by Oxoid U.S.A., Inc.. It is a Class 1 Toxicology device (product code JSI) cleared through the Traditional 510(k) pathway after a 27-day FDA review.

K811514 · Oxoid U.S.A., Inc. · Toxicology device
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Jun 1981
Decision
27d
Days
Class 1
Risk

K811514 is an FDA 510(k) clearance for the BACILLUS CEREUS SELECTIVE(AGAR&SUPP). Classified as Culture Media, Selective And Differential (product code JSI), Class I - General Controls.

Submitted by Oxoid U.S.A., Inc. (Mchenry, US). The FDA issued a Cleared decision on June 24, 1981 after a review of 27 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 866.2360 - the FDA toxicology 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 Oxoid U.S.A., Inc. devices

Submission Details

510(k) Number K811514 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 28, 1981
Decision Date June 24, 1981
Days to Decision 27 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
60d faster than avg
Panel avg: 87d · This submission: 27d
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 187
Devices cleared under the same product code (JSI) and FDA review panel - the closest regulatory comparables to K811514.
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MINERALS MODIFIED MED. BASE & SOD. GLUT.
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SF BROTH
K811331 · Acumedia Manufacturers, Inc. · May 1981
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K811332 · Acumedia Manufacturers, Inc. · May 1981