GENDER CHOICE INFORMATION KIT, FEMALE AND MALE— 510(k) K870999
Substantially EquivalentProcare C/O Wiley, Rein & Fielding
FDA 510(k) clearance K870999 for GENDER CHOICE INFORMATION KIT, FEMALE AND MALE, Substantially Equivalent on 1987-07-14. Applicant: Procare C/O Wiley, Rein & Fielding.
Clearance details
- Applicant
- Procare C/O Wiley, Rein & Fielding
- Product code
- Code LHD
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.