INTRAUTERINE DEVICE REMOVER— 510(k) K842295
Substantially EquivalentPremier Dental Products Co.
FDA 510(k) clearance K842295 for INTRAUTERINE DEVICE REMOVER, Substantially Equivalent on 1984-10-12. Applicant: Premier Dental Products Co..
Clearance details
- Applicant
- Premier Dental Products Co.
- Product code
- Code HHF
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Norristown, PA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.