ELASTIC COMPRESSION ANKLET— 510(k) K823350
Substantially EquivalentPodiatry Products Corp.
FDA 510(k) clearance K823350 for ELASTIC COMPRESSION ANKLET, Substantially Equivalent on 1982-12-03. Applicant: Podiatry Products Corp..
Clearance details
- Applicant
- Podiatry Products Corp.
- Product code
- Code FQL
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Adverse events under product code FQL
product code FQL- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . 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.