PARALLEL— 510(k) K954007

Name: FDA 510(k) clearance K954007
Creator: U.S. Food and Drug Administration
Published: 1995-11-22

Substantially Equivalent

Johnson & Johnson Consumer Products, Inc.

FDA 510(k) clearance K954007 for PARALLEL, Substantially Equivalent on 1995-11-22. Applicant: Johnson & Johnson Consumer Products, Inc.. Device class: 1.

Clearance details

Applicant: Johnson & Johnson Consumer Products, Inc.
Product code: Code KGX
Device class: Class 1
Regulation: 21 CFR 880.5240
Advisory panel: General Hospital
Date received: 1995-08-25
Decision date: 1995-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Skillman, NJ, US

Download summary PDF View on FDA.gov ↗

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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.