Cleared Traditional

K852873 - CEFTAZIDIME 30MCG. SENI-DISC (FDA 510(k) Clearance)

Aug 1985
Decision
42d
Days
Class 2
Risk

K852873 is an FDA 510(k) clearance for the CEFTAZIDIME 30MCG. SENI-DISC. This device is classified as a Susceptibility Test Discs, Antimicrobial (Class II - Special Controls, product code JTN).

Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Paramus, US). The FDA issued a Cleared decision on August 19, 1985, 42 days after receiving the submission on July 8, 1985.

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

Submission Details

510(k) Number K852873 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 08, 1985
Decision Date August 19, 1985
Days to Decision 42 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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