DERMIVIEW CLEAR TAPE— 510(k) K942383

Name: FDA 510(k) clearance K942383
Creator: U.S. Food and Drug Administration
Published: 1994-08-22

Substantially Equivalent

Johnson & Johnson International

FDA 510(k) clearance K942383 for DERMIVIEW CLEAR TAPE, Substantially Equivalent on 1994-08-22. Applicant: Johnson & Johnson International. Device class: 1.

Clearance details

Applicant: Johnson & Johnson International
Product code: Code KGX
Device class: Class 1
Regulation: 21 CFR 880.5240
Advisory panel: General Hospital
Date received: 1994-05-19
Decision date: 1994-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington, TX, US

Download summary PDF View on FDA.gov ↗

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K952606 — TARGETT PATCH1995-12-21

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Adverse events under product code KGX

product code KGX

Injury: 1,590
Malfunction: 1,357
Other: 3
Total: 2,950

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.