Cleared Traditional

K860410 - BIOTIS COOKED MEAT

K860410 is the FDA 510(k) clearance for BIOTIS COOKED MEAT by Otisville Biotech, Inc.. It is a Class 1 Microbiology device (product code KZI) cleared through the Traditional 510(k) pathway after a 21-day FDA review.

K860410 · Otisville Biotech, Inc. · Microbiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1986
Decision
21d
Days
Class 1
Risk

K860410 is an FDA 510(k) clearance for the BIOTIS COOKED MEAT. Classified as Culture Media, Enriched (product code KZI), 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 866.2330 - 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 K860410 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 KZI Culture Media, Enriched
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2330
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 - KZI Culture Media, Enriched

All 29
Devices cleared under the same product code (KZI) and FDA review panel - the closest regulatory comparables to K860410.
LOMBARD DOWELL AGAR BASE
K864014 · Gibco Laboratories Life Technologies, Inc. · Oct 1986
VACUTAINER BRAND AGAR SLANT
K862761 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Aug 1986
BIOTIS BORDET GENGOU AGAR
K862390 · Otisville Biotech, Inc. · Jul 1986
BCYE (BUFFERED CHARCOAL YEAST EXTRACT) AGAR
K854064 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Oct 1985
BIOTIS CDC MODIFIED MCCLUNG-TOABE EGG
K843065 · Otisville Biotech, Inc. · Aug 1984
SELENITE CYSTINE BROTH
K832533 · Otisville Biotech, Inc. · Oct 1983