L-5 PLASTIC SURGERY CANNULAS— 510(k) K880669
Substantially EquivalentAmerican Instrument Manufacturer'S, Inc.
FDA 510(k) clearance K880669 for L-5 PLASTIC SURGERY CANNULAS, Substantially Equivalent on 1988-03-17. Applicant: American Instrument Manufacturer'S, Inc..
Clearance details
- Applicant
- American Instrument Manufacturer'S, Inc.
- Product code
- Code GEA
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Eureka, MO, US
Adverse events under product code GEA
product code GEA- Malfunction
- 587
- Total
- 587
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.