VALLEY FORGE BIPOLAR LOOP— 510(k) K971986
Substantially EquivalentValley Forge Scientific Corp.
FDA 510(k) clearance K971986 for VALLEY FORGE BIPOLAR LOOP, Substantially Equivalent on 1997-08-26. Applicant: Valley Forge Scientific Corp..
Clearance details
- Applicant
- Valley Forge Scientific Corp.
- Product code
- Code HGI
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Oaks, PA, 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.