Cleared Traditional

K945883 - LYFO(TM) DIFFERENTIAL DISK-BILE ESCULIN

K945883 is an FDA 510(k) clearance for LYFO(TM) DIFFERENTIAL DISK-BILE ESCULIN, manufactured by Microbiologics, Inc.. The device is a Class 1 Microbiology device with product code JTO cleared through the Traditional 510(k) pathway after a 144-day FDA review.

K945883 · Microbiologics, Inc. · Microbiology device
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Apr 1995
Decision
144d
Days
Class 1
Risk

K945883 is an FDA 510(k) clearance for the LYFO(TM) DIFFERENTIAL DISK-BILE ESCULIN. Classified as Discs, Strips And Reagents, Microorganism Differentiation (product code JTO), Class I - General Controls.

Submitted by Microbiologics, Inc. (St. Cloud, US). The FDA issued a Cleared decision on April 24, 1995 after a review of 144 days - within the typical 510(k) review window.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2660 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Microbiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Microbiologics, Inc. devices

FDA 510(k) Submission Details - K945883

510(k) Number K945883 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 01, 1994
Decision Date April 24, 1995
Days to Decision 144 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
42d slower than avg
Panel avg: 102d · This submission: 144d
Pathway characteristics
Predicate-based equivalence.

JTO Device Classification - Class 1, General Controls

Product Code JTO Discs, Strips And Reagents, Microorganism Differentiation
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2660
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 - JTO Discs, Strips And Reagents, Microorganism Differentiation

All 195
Devices cleared under the same product code (JTO) and FDA review panel - the closest regulatory comparables to K945883.
LYFO(TM) DIFFERENTIAL DISK-SPS
K945880 · Microbiologics, Inc. · Apr 1995
LYFO(TM) DIFFERENTIAL DISK-STERILE DISK
K945881 · Microbiologics, Inc. · Apr 1995
LYFO(TM) DIFFERENTIAL DISK-BILE
K945882 · Microbiologics, Inc. · Apr 1995
DISPENS-O-DISC(TM) NITROCEFIN
K941016 · Difco Laboratories, Inc. · Jun 1994
BACTICARD STREP
K936021 · Remel Co. · May 1994
SERIM PYLORITEK REAGENT STRIPS
K936034 · Serim Research Corp. · Apr 1994