Cleared Traditional

K860414 - BIOTIS ORNITHINE INDOLE MOTILITY MEDIA

K860414 is the FDA 510(k) clearance for BIOTIS ORNITHINE INDOLE MOTILITY MEDIA by Otisville Biotech, Inc.. It is a Class 1 Microbiology device (product code JSE) cleared through the Traditional 510(k) pathway after a 21-day FDA review.

K860414 · Otisville Biotech, Inc. · Microbiology device
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Feb 1986
Decision
21d
Days
Class 1
Risk

K860414 is an FDA 510(k) clearance for the BIOTIS ORNITHINE INDOLE MOTILITY MEDIA. Classified as Culture Media, Multiple Biochemical Test (product code JSE), Class I - General Controls.

Submitted by Otisville Biotech, Inc. (Otisville, US). The FDA issued a Cleared decision on February 24, 1986 after a review of 21 days - a notably fast clearance 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: 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 Otisville Biotech, Inc. devices

Submission Details

510(k) Number K860414 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 03, 1986
Decision Date February 24, 1986
Days to Decision 21 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
81d faster than avg
Panel avg: 102d · This submission: 21d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JSE Culture Media, Multiple Biochemical Test
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 - JSE Culture Media, Multiple Biochemical Test

All 38
Devices cleared under the same product code (JSE) and FDA review panel - the closest regulatory comparables to K860414.
BIOTIS LITMUS MILK
K862393 · Otisville Biotech, Inc. · Jul 1986
BIOTIS SIM MEDIUM
K860412 · Otisville Biotech, Inc. · Feb 1986
BIOTIS TSI
K860413 · Otisville Biotech, Inc. · Feb 1986
BIOTIS SIMMON CITRATE AGAR
K860415 · Otisville Biotech, Inc. · Feb 1986
AUSTIN ENTERIC SYSTEM
K860194 · Austin Biological Laboratories · Feb 1986
CTAPI - NEISSERA SCREEN
K850982 · Analytical Products, Inc. · Mar 1985