BOWEN ELECTRODE SKIN PREPATORY CLEANSER— 510(k) K896898

Name: FDA 510(k) clearance K896898
Creator: U.S. Food and Drug Administration
Published: 1990-04-04

Substantially Equivalent

Bowen & Company, Inc.

FDA 510(k) clearance K896898 for BOWEN ELECTRODE SKIN PREPATORY CLEANSER, Substantially Equivalent on 1990-04-04. Applicant: Bowen & Company, Inc.. Device class: Unclassified.

Clearance details

Applicant: Bowen & Company, Inc.
Product code: Code LKB
Device class: Unclassified
Advisory panel: Unknown
Date received: 1989-12-08
Decision date: 1990-04-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockville, MD, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LKB

product code LKB

Other: 2
Total: 2

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.