COPD LIQUID OXYGEN PORTABLE, MODEL 300P— 510(k) K072011
Substantially EquivalentCopd Partners, Inc.
FDA 510(k) clearance K072011 for COPD LIQUID OXYGEN PORTABLE, MODEL 300P, Substantially Equivalent on 2007-10-18. Applicant: Copd Partners, Inc..
Clearance details
- Applicant
- Copd Partners, Inc.
- Product code
- Code BYJ
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bonita Springs, FL, US
Adverse events under product code BYJ
product code BYJ- Death
- 16
- Total
- 16
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.