Cleared Traditional

K103028 - EEVATM PETRI DISH

K103028 is an FDA 510(k) clearance for EEVATM PETRI DISH, manufactured by Auxogyn, Inc.. The device is a Class 2 Obstetrics & Gynecology device with product code MQK cleared through the Traditional 510(k) pathway after a 302-day FDA review.

K103028 · Auxogyn, Inc. · Obstetrics & Gynecology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2011
Decision
302d
Days
Class 2
Risk

K103028 is an FDA 510(k) clearance for the EEVATM PETRI DISH. Classified as Labware, Assisted Reproduction (product code MQK), Class II - Special Controls.

Submitted by Auxogyn, Inc. (Menlo Park, US). The FDA issued a Cleared decision on August 11, 2011 after a review of 302 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.6160 - the FDA obstetrics and gynecology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Elevated predicate reliance profile. This clearance follows a standard predicate-based equivalence path within the Obstetrics & Gynecology review framework, consistent with the majority of Class II 510(k) submissions.

View all Auxogyn, Inc. devices

FDA 510(k) Submission Details - K103028

510(k) Number K103028 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 13, 2010
Decision Date August 11, 2011
Days to Decision 302 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
142d slower than avg
Panel avg: 160d · This submission: 302d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MQK Device Classification - Class 2, Special Controls

Product Code MQK Labware, Assisted Reproduction
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.6160
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Obstetrics & Gynecology devices follow this clearance model.

Regulatory Peers - MQK Labware, Assisted Reproduction

All 41
Devices cleared under the same product code (MQK) and FDA review panel - the closest regulatory comparables to K103028.
SEAFORIA SPERM SEPARATION ASSISTANCE SYSTEM
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CRYOTOP
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RI MSC (MIGRATION SEDIMENTATION CHAMBER)
K112413 · Research Instruments , Ltd. · Jul 2012
RAPID-I
K090832 · Vitrolife Sweden AB · Dec 2009
SUNIVF DISHES
K080395 · Intl., Inc. · Aug 2008
ESP FOUR WELL TISSUE CULTURE PLATE, ESP SIX WELL TISSUE CULTURE PLATE, ESP MICRO SIX WELL TISSUE CULTURE PLATE, ESP WELL
K994361 · Genesis Industries, Inc. · Feb 2000