Cleared Traditional

K831179 - CEFAZOLIN 30MCG. ANTIMICROBIAL SUSCEP
(FDA 510(k) Clearance)

May 1983
Decision
28d
Days
Class 2
Risk

K831179 is an FDA 510(k) clearance for the CEFAZOLIN 30MCG. ANTIMICROBIAL SUSCEP. This device is classified as a Susceptibility Test Discs, Antimicrobial (Class II - Special Controls, product code JTN).

Submitted by General Diagnostics (Mchenry, US). The FDA issued a Cleared decision on May 9, 1983, 28 days after receiving the submission on April 11, 1983.

This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.1620.

Submission Details

510(k) Number K831179 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 11, 1983
Decision Date May 09, 1983
Days to Decision 28 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary

Device Classification

Product Code JTN — Susceptibility Test Discs, Antimicrobial
Device Class Class II - Special Controls
CFR Regulation 21 CFR 866.1620

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