Cleared Traditional

MODEL LS-85 & MEDEL 1828 LINESCAN VISCO

K822926 · Honeywell, Inc. · Cardiovascular

Nov 1982

Decision

54d

Days

—

Risk

About This 510(k) Submission

K822926 is an FDA 510(k) clearance for the MODEL LS-85 & MEDEL 1828 LINESCAN VISCO, submitted by Honeywell, Inc. (Walker, US). The FDA issued a Cleared decision on November 24, 1982, 54 days after receiving the submission on October 1, 1982. This device falls under the Cardiovascular review panel.

Submission Details

510(k) Number	K822926 FDA.gov
FDA Decision	Cleared SESE
Date Received	October 01, 1982
Decision Date	November 24, 1982
Days to Decision	54 days
Submission Type	Traditional
Review Panel	Cardiovascular (CV)
Summary	—