PODOFLEX EXERCISER-PASSIVE-FOOT/ANKLE— 510(k) K901796

Name: FDA 510(k) clearance K901796
Creator: U.S. Food and Drug Administration
Published: 1990-06-06

Substantially Equivalent

Component Equipment Mfg., Inc.

FDA 510(k) clearance K901796 for PODOFLEX EXERCISER-PASSIVE-FOOT/ANKLE, Substantially Equivalent on 1990-06-06. Applicant: Component Equipment Mfg., Inc.. Device class: 1.

Clearance details

Applicant: Component Equipment Mfg., Inc.
Product code: Code ISA
Device class: Class 1
Regulation: 21 CFR 890.5660
Advisory panel: Physical Medicine
Date received: 1990-04-19
Decision date: 1990-06-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Colorado Springs, CO, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code ISA

product code ISA

Death: 3
Other: 1
Total: 4

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.