Cleared Traditional

K000915 - PASTEUR PIPET - STERILE 9, PASTEUR PIPET - STERILE 5 3/4, MODELS 16-PP-9, 16-PP-5.75

K000915 is an FDA 510(k) clearance for PASTEUR PIPET - STERILE 9, manufactured by Humagen Fertility Diagnostics, Inc.. The device is a Class 2 Obstetrics & Gynecology device with product code MQK cleared through the Traditional 510(k) pathway after a 51-day FDA review.

K000915 · Humagen Fertility Diagnostics, Inc. · Obstetrics & Gynecology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2000
Decision
51d
Days
Class 2
Risk

K000915 is an FDA 510(k) clearance for the PASTEUR PIPET - STERILE 9, PASTEUR PIPET - STERILE 5 3/4, MODELS 16-PP-9, 16-.... Classified as Labware, Assisted Reproduction (product code MQK), Class II - Special Controls.

Submitted by Humagen Fertility Diagnostics, Inc. (Charlottesville, US). The FDA issued a Cleared decision on May 12, 2000 after a review of 51 days - a notably fast clearance cycle.

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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Humagen Fertility Diagnostics, Inc. devices

FDA 510(k) Submission Details - K000915

510(k) Number K000915 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 22, 2000
Decision Date May 12, 2000
Days to Decision 51 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
109d faster than avg
Panel avg: 160d · This submission: 51d
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 26
Devices cleared under the same product code (MQK) and FDA review panel - the closest regulatory comparables to K000915.
RAPID-I KIT
K140207 · Vitrolife Sweden AB · Dec 2014
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
GENX CULTURE DISH
K993881 · Intl., Inc. · Feb 2000
NEWLIFE DISH (ETCHED OR NON-ETCHED, WITH OR WITHOUT LID), MODELS 14-52, 1452E, 1452EL, 1452L
K990941 · Humagen Fertility Diagnostics, Inc. · Jul 1999