TUCKER EMBRYO CATHETER— 510(k) K023017
Substantially EquivalentFertility Technology Resources, Inc.
FDA 510(k) clearance K023017 for TUCKER EMBRYO CATHETER, Substantially Equivalent on 2002-12-13. Applicant: Fertility Technology Resources, Inc.. Device class: 2.
Clearance details
- Applicant
- Fertility Technology Resources, Inc.
- Product code
- Code MQF
- Device class
- Class 2
- Regulation
- 21 CFR 884.6110
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Marietta, GA, US
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More clearances from Fertility Technology Resources, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.