Cleared Traditional

K842947 - MICROBIOLOGICAL TRAY READER-MANUAL

K842947 is the FDA 510(k) clearance for MICROBIOLOGICAL TRAY READER-MANUAL by American Micro Scan. It is a Class 1 Microbiology device (product code JJQ) cleared through the Traditional 510(k) pathway after a 50-day FDA review.

K842947 · American Micro Scan · Microbiology device
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Sep 1984
Decision
50d
Days
Class 1
Risk

K842947 is an FDA 510(k) clearance for the MICROBIOLOGICAL TRAY READER-MANUAL. Classified as Colorimeter, Photometer, Spectrophotometer For Clinical Use (product code JJQ), Class I - General Controls.

Submitted by American Micro Scan (Mchenry, US). The FDA issued a Cleared decision on September 14, 1984 after a review of 50 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 862.2300 - 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 American Micro Scan devices

Submission Details

510(k) Number K842947 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 26, 1984
Decision Date September 14, 1984
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.

Device Classification

Product Code JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.2300
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 - JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use

All 135
Devices cleared under the same product code (JJQ) and FDA review panel - the closest regulatory comparables to K842947.
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