MODIFIED HOMECLINIC PREGNANCY TEST— 510(k) K895560
Substantially EquivalentVanguard Biomedical Corp.
FDA 510(k) clearance K895560 for MODIFIED HOMECLINIC PREGNANCY TEST, Substantially Equivalent on 1989-11-13. Applicant: Vanguard Biomedical Corp.. Device class: 2.
Clearance details
- Applicant
- Vanguard Biomedical Corp.
- Product code
- Code LCX
- Device class
- Class 2
- Regulation
- 21 CFR 862.1155
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Recent devices under product code LCX
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- K243573 — FaStep Early Pregnancy Rapid Test Strip +2 more
More clearances from Vanguard Biomedical Corp.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.