AART SILICONE SHEETING— 510(k) K022223
Substantially EquivalentAesthetic and Reconstructive Technologies, Inc.
FDA 510(k) clearance K022223 for AART SILICONE SHEETING, Substantially Equivalent on 2002-08-08. Applicant: Aesthetic and Reconstructive Technologies, Inc..
Clearance details
- Applicant
- Aesthetic and Reconstructive Technologies, Inc.
- Product code
- Code MIB
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Paso Robles, CA, US
Adverse events under product code MIB
product code MIB- Injury
- 146
- Total
- 146
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.