Cleared Traditional

K874177 - BIOTIS (TM) BCYE

K874177 is an FDA 510(k) clearance for BIOTIS (TM) BCYE, manufactured by Otisville Biopharm, Inc.. The device is a Class 1 Microbiology device with product code KZI cleared through the Traditional 510(k) pathway after a 50-day FDA review.

K874177 · Otisville Biopharm, Inc. · Microbiology device
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Dec 1987
Decision
50d
Days
Class 1
Risk

K874177 is an FDA 510(k) clearance for the BIOTIS (TM) BCYE. Classified as Culture Media, Enriched (product code KZI), Class I - General Controls.

Submitted by Otisville Biopharm, Inc. (Otisville, US). The FDA issued a Cleared decision on December 4, 1987 after a review of 50 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 Biopharm, Inc. devices

FDA 510(k) Submission Details - K874177

510(k) Number K874177 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 15, 1987
Decision Date December 04, 1987
Days to Decision 50 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
52d faster than avg
Panel avg: 102d · This submission: 50d
Pathway characteristics
Predicate-based equivalence.

KZI Device Classification - Class 1, General Controls

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 38
Devices cleared under the same product code (KZI) and FDA review panel - the closest regulatory comparables to K874177.
CYSTINE TRYPTIC MEDIUM BASE
K880109 · Hardy Media · Mar 1988
WALLENSTEIN MEDIUM SLANT
K880138 · Hardy Media · Mar 1988
POTATO DEXTROSE AGAR
K880127 · Hardy Media · Mar 1988
MICRO CULTURE MEDIA P3141, P3136, P3148, P3748
K873952 · Lakewood Biochemical Co., Inc. · Oct 1987
SABOURAUD DEXTR/BHI SD/BHI AGAR SLT W/6% SHEEP BLD
K873320 · Lakewood Biochemical Co., Inc. · Sep 1987
SABOUR DEXTROSE/BHI SD/BHI AGAR SLT TUBE #T4300
K873321 · Lakewood Biochemical Co., Inc. · Sep 1987