OXYCON— 510(k) K813436
Substantially EquivalentHome Medical Mfg., Co., Inc.
FDA 510(k) clearance K813436 for OXYCON, Substantially Equivalent on 1982-01-07. Applicant: Home Medical Mfg., Co., Inc.. Device class: 2.
Clearance details
- Applicant
- Home Medical Mfg., Co., Inc.
- Product code
- Code CAW
- Device class
- Class 2
- Regulation
- 21 CFR 868.5440
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code CAW
view allAdverse events under product code CAW
product code CAW- Death
- 204
- Injury
- 573
- Malfunction
- 1,400
- Other
- 6
- Total
- 2,183
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.