Cleared Traditional

K862387 - BIOTIS HAEMOPHILUS IDENTIFICATION QUAD

K862387 is the FDA 510(k) clearance for BIOTIS HAEMOPHILUS IDENTIFICATION QUAD by Otisville Biotech, Inc.. It is a Class 1 Microbiology device (product code JSH) cleared through the Traditional 510(k) pathway after a 9-day FDA review.

K862387 · Otisville Biotech, Inc. · Microbiology device
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Jul 1986
Decision
9d
Days
Class 1
Risk

K862387 is an FDA 510(k) clearance for the BIOTIS HAEMOPHILUS IDENTIFICATION QUAD. Classified as Culture Media, Non-selective And Differential (product code JSH), Class I - General Controls.

Submitted by Otisville Biotech, Inc. (Otisville, US). The FDA issued a Cleared decision on July 3, 1986 after a review of 9 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 K862387 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 24, 1986
Decision Date July 03, 1986
Days to Decision 9 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
93d faster than avg
Panel avg: 102d · This submission: 9d
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 101
Devices cleared under the same product code (JSH) and FDA review panel - the closest regulatory comparables to K862387.
STARCH AGAR W/BROM CRESOL PURPLE
K863599 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Sep 1986
MOTILITY INDOLE LYSINE SULFIDE (MILS) MEDIUM
K863600 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Sep 1986
TOC (TWEEN 80 - OXGALL-CAFFEIC ACID) AGAR
K863523 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Sep 1986
BIOTIS DECARBOXYLASE MEDIA, BASE
K862395 · Otisville Biotech, Inc. · Jul 1986
PSEUDOMONAS AGAR P (MEDIUM A)
K860750 · Gibco Laboratories Life Technologies, Inc. · Mar 1986
DNASE W/TOLUIDINE BLUE, DNASE W/INDICATOR
K853336 · Hardy Media · Aug 1985