ANAGO FEM-COOL/FEM-COOL PETITE— 510(k) K926137

Name: FDA 510(k) clearance K926137
Creator: U.S. Food and Drug Administration
Published: 1993-05-26

Substantially Equivalent

Anago, Inc.

FDA 510(k) clearance K926137 for ANAGO FEM-COOL/FEM-COOL PETITE, Substantially Equivalent on 1993-05-26. Applicant: Anago, Inc.. Device class: 1.

Clearance details

Applicant: Anago, Inc.
Product code: Code IMD
Device class: Class 1
Regulation: 21 CFR 890.5710
Advisory panel: Physical Medicine
Date received: 1992-12-07
Decision date: 1993-05-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Worth, TX, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code IMD

product code IMD

Death: 3
Injury: 600
Total: 603

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.