EEVATM PETRI DISH— 510(k) K103028
Substantially EquivalentAuxogyn, Inc.
FDA 510(k) clearance K103028 for EEVATM PETRI DISH, Substantially Equivalent on 2011-08-11. Applicant: Auxogyn, Inc.. Device class: 2.
Clearance details
- Applicant
- Auxogyn, 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
- Menlo Park, CA, US
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More clearances from Auxogyn, Inc.
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