MOPYLEN— 510(k) K922630

Name: FDA 510(k) clearance K922630
Creator: U.S. Food and Drug Administration
Published: 1992-10-20

Substantially Equivalent

S. Jackson, Inc.

FDA 510(k) clearance K922630 for MOPYLEN, Substantially Equivalent on 1992-10-20. Applicant: S. Jackson, Inc.. Device class: 2.

Clearance details

Applicant: S. Jackson, Inc.
Product code: Code GAW
Device class: Class 2
Regulation: 21 CFR 878.5010
Advisory panel: General, Plastic Surgery
Date received: 1992-06-03
Decision date: 1992-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alexandria, VA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GAW

product code GAW

Death: 66
Injury: 1,616
Malfunction: 10,428
Total: 12,110

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.