Cleared Traditional

SECHRIST VOLUME VENTILATOR MODIFICATION

K850740 · Sechrist Industries, Inc. · Cardiovascular

Jul 1985

Decision

182d

Days

—

Risk

About This 510(k) Submission

K850740 is an FDA 510(k) clearance for the SECHRIST VOLUME VENTILATOR MODIFICATION, submitted by Sechrist Industries, Inc. (Anaheim, US). The FDA issued a Cleared decision on July 29, 1985, 182 days after receiving the submission on January 28, 1985. This device falls under the Cardiovascular review panel.

Submission Details

510(k) Number	K850740 FDA.gov
FDA Decision	Cleared SESE
Date Received	January 28, 1985
Decision Date	July 29, 1985
Days to Decision	182 days
Submission Type	Traditional
Review Panel	Cardiovascular (CV)
Summary	—