Cleared Traditional

K854448 - AUTOSCAN W/A SYSTEM
(FDA 510(k) Clearance)

Nov 1985
Decision
21d
Days
Class 1
Risk

K854448 is an FDA 510(k) clearance for the AUTOSCAN W/A SYSTEM. This device is classified as a Discs, Strips And Reagents, Microorganism Differentiation (Class I - General Controls, product code JTO).

Submitted by American Micro Scan (Sacramento, US). The FDA issued a Cleared decision on November 26, 1985, 21 days after receiving the submission on November 5, 1985.

This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.2660.

Submission Details

510(k) Number K854448 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 05, 1985
Decision Date November 26, 1985
Days to Decision 21 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary

Device Classification

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