GENX CULTURE DISH— 510(k) K993881
Substantially Equivalent<Genx> Intl., Inc.
FDA 510(k) clearance K993881 for GENX CULTURE DISH, Substantially Equivalent on 2000-02-14. Applicant: <Genx> Intl., Inc.. Device class: 2.
Clearance details
- Applicant
- <Genx> Intl., Inc.
- Product code
- Code MQK
- Device class
- Class 2
- Regulation
- 21 CFR 884.6160
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Madison, CT, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.