PHASIX-HIGH FREQUENCY GENERATOR— 510(k) K834306
Substantially EquivalentCgr Medical Corp.
FDA 510(k) clearance K834306 for PHASIX-HIGH FREQUENCY GENERATOR, Substantially Equivalent on 1983-12-29. Applicant: Cgr Medical Corp..
Clearance details
- Applicant
- Cgr Medical Corp.
- Product code
- Code ITY
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Adverse events under product code ITY
product code ITY- 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.