Cleared Traditional

K842279 - BECTEC NR-660 BACTERIAL DETECT SYS (FDA 510(k) Clearance)

Jul 1984
Decision
42d
Days
Class 1
Risk

K842279 is an FDA 510(k) clearance for the BECTEC NR-660 BACTERIAL DETECT SYS. This device is classified as a Monitor, Microbial Growth (Class I - General Controls, product code JTA).

Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Walker, US). The FDA issued a Cleared decision on July 20, 1984, 42 days after receiving the submission on June 8, 1984.

This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.2560.

Submission Details

510(k) Number K842279 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 08, 1984
Decision Date July 20, 1984
Days to Decision 42 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary

Device Classification

Product Code JTA — Monitor, Microbial Growth
Device Class Class I - General Controls
CFR Regulation 21 CFR 866.2560