Cleared Traditional

K823479 - MODUFLEX NEONATAL VENTILATOR SET (FDA 510(k) Clearance)

Dec 1982
Decision
22d
Days
Class 1
Risk

K823479 is an FDA 510(k) clearance for the MODUFLEX NEONATAL VENTILATOR SET. This device is classified as a Set, Tubing And Support, Ventilator (w Harness) (Class I - General Controls, product code BZO).

Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Washington, US). The FDA issued a Cleared decision on December 15, 1982, 22 days after receiving the submission on November 23, 1982.

This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5975.

Submission Details

510(k) Number K823479 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 23, 1982
Decision Date December 15, 1982
Days to Decision 22 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary

Device Classification

Product Code BZO — Set, Tubing And Support, Ventilator (w Harness)
Device Class Class I - General Controls
CFR Regulation 21 CFR 868.5975