Cleared Traditional

MAXI-MISER HUMIDIFIER INSERT 1020

K841569 · Nova-Ventrx · Cardiovascular

May 1984

Decision

43d

Days

—

Risk

About This 510(k) Submission

K841569 is an FDA 510(k) clearance for the MAXI-MISER HUMIDIFIER INSERT 1020, submitted by Nova-Ventrx (Mchenry, US). The FDA issued a Cleared decision on May 30, 1984, 43 days after receiving the submission on April 17, 1984. This device falls under the Cardiovascular review panel.

Submission Details

510(k) Number	K841569 FDA.gov
FDA Decision	Cleared SESE
Date Received	April 17, 1984
Decision Date	May 30, 1984
Days to Decision	43 days
Submission Type	Traditional
Review Panel	Cardiovascular (CV)
Summary	—