MODEL 80-1983, ELECTROSURGICAL GENERATOR— 510(k) K931437
Substantially EquivalentCameron-Miller, Inc.
FDA 510(k) clearance K931437 for MODEL 80-1983, ELECTROSURGICAL GENERATOR, Substantially Equivalent on 1994-05-27. Applicant: Cameron-Miller, Inc..
Clearance details
- Applicant
- Cameron-Miller, Inc.
- Product code
- Code HGI
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chicago, IL, US
Adverse events under product code HGI
product code HGI- 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.