FERTELL FEMALE FERTILITY TEST— 510(k) K032002
Substantially EquivalentGenosis, Inc.
FDA 510(k) clearance K032002 for FERTELL FEMALE FERTILITY TEST, Substantially Equivalent on 2003-10-30. Applicant: Genosis, Inc.. Device class: 1.
Clearance details
- Applicant
- Genosis, Inc.
- Product code
- Code NGA
- Device class
- Class 1
- Regulation
- 21 CFR 862.1300
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Recent devices under product code NGA
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