Cleared Traditional

BOWEN ELECTRODE SKIN PREPATORY CLEANSER

K896898 · Bowen & Company, Inc. · General Hospital
Apr 1990
Decision
117d
Days
—
Risk

About This 510(k) Submission

K896898 is an FDA 510(k) clearance for the BOWEN ELECTRODE SKIN PREPATORY CLEANSER, a Pad, Alcohol, Device Disinfectant, submitted by Bowen & Company, Inc. (Rockville, US). The FDA issued a Cleared decision on April 4, 1990, 117 days after receiving the submission on December 8, 1989. This device falls under the General Hospital review panel.

Submission Details

510(k) Number K896898 FDA.gov
FDA Decision Cleared SESE
Date Received December 08, 1989
Decision Date April 04, 1990
Days to Decision 117 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary —

Device Classification

Product Code LKB — Pad, Alcohol, Device Disinfectant
Device Class —