ENVIVE MINIFORMS— 510(k) K003843
Substantially EquivalentProcter & Gamble Co.
FDA 510(k) clearance K003843 for ENVIVE MINIFORMS, Substantially Equivalent on 2001-02-08. Applicant: Procter & Gamble Co.. Device class: 1.
Clearance details
- Applicant
- Procter & Gamble Co.
- Product code
- Code HHD
- Device class
- Class 1
- Regulation
- 21 CFR 884.5435
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cincinnati, OH, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.