Cleared Traditional

K853380 - SPR 2 AUTODILUTER

K853380 is an FDA 510(k) clearance for SPR 2 AUTODILUTER, manufactured by Scientific Sales Intl., Inc.. The device is a Class 1 Microbiology device with product code JTC cleared through the Traditional 510(k) pathway after a 31-day FDA review.

K853380 · Scientific Sales Intl., Inc. · Microbiology device
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Sep 1985
Decision
31d
Days
Class 1
Risk

K853380 is an FDA 510(k) clearance for the SPR 2 AUTODILUTER. Classified as Device, Microtiter Diluting/dispensing (product code JTC), Class I - General Controls.

Submitted by Scientific Sales Intl., Inc. (Kalamazoo, US). The FDA issued a Cleared decision on September 12, 1985 after a review of 31 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2500 - 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 Scientific Sales Intl., Inc. devices

FDA 510(k) Submission Details - K853380

510(k) Number K853380 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 12, 1985
Decision Date September 12, 1985
Days to Decision 31 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
71d faster than avg
Panel avg: 102d · This submission: 31d
Pathway characteristics
Predicate-based equivalence.

JTC Device Classification - Class 1, General Controls

Product Code JTC Device, Microtiter Diluting/dispensing
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.2500
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 - JTC Device, Microtiter Diluting/dispensing

All 37
Devices cleared under the same product code (JTC) and FDA review panel - the closest regulatory comparables to K853380.
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