Cleared Traditional

K844540 - CYSTINE TRYPTIC AGAR W/FRUCTOSE (FDA 510(k) Clearance)

Jan 1985
Decision
47d
Days
Class 1
Risk

K844540 is an FDA 510(k) clearance for the CYSTINE TRYPTIC AGAR W/FRUCTOSE. This device is classified as a Culture Media, Single Biochemical Test (Class I - General Controls, product code JSF).

Submitted by bioMerieux, Inc. (Addison, US). The FDA issued a Cleared decision on January 7, 1985, 47 days after receiving the submission on November 21, 1984.

This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.2320.

Submission Details

510(k) Number K844540 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 21, 1984
Decision Date January 07, 1985
Days to Decision 47 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary

Device Classification

Product Code JSF — Culture Media, Single Biochemical Test
Device Class Class I - General Controls
CFR Regulation 21 CFR 866.2320