Cleared Traditional

K030850 - ENHANCE HUMAN SERUM ALBUMIN

K030850 is an FDA 510(k) clearance for ENHANCE HUMAN SERUM ALBUMIN, manufactured by Conception Technologies. The device is a Class 2 Obstetrics & Gynecology device with product code MQL cleared through the Traditional 510(k) pathway after a 22-day FDA review.

K030850 · Conception Technologies · Obstetrics & Gynecology device
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Apr 2003
Decision
22d
Days
Class 2
Risk

K030850 is an FDA 510(k) clearance for the ENHANCE HUMAN SERUM ALBUMIN. Classified as Media, Reproductive (product code MQL), Class II - Special Controls.

Submitted by Conception Technologies (Irvine, US). The FDA issued a Cleared decision on April 8, 2003 after a review of 22 days - a notably fast clearance cycle.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.6180 - 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 Conception Technologies devices

FDA 510(k) Submission Details - K030850

510(k) Number K030850 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 17, 2003
Decision Date April 08, 2003
Days to Decision 22 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
138d faster than avg
Panel avg: 160d · This submission: 22d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MQL Device Classification - Class 2, Special Controls

Product Code MQL Media, Reproductive
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.6180
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 - MQL Media, Reproductive

All 197
Devices cleared under the same product code (MQL) and FDA review panel - the closest regulatory comparables to K030850.
BLASTFREEZE AND BLASTTHAW
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K031228 · Medicult A/S · Jun 2003
EMBRYOGLUE
K031015 · Vitrolife Sweden AB · Jun 2003
SYDNEY IVF EMBRYO BIOPSY MEDIUM
K023850 · Cook Ob/Gyn · Jan 2003
SYDNEY IVF HYALURONIDASE
K023353 · Cook Urological, Inc. · Dec 2002
SPERMGRAD, MODELS 10022/10063
K023403 · Vitrolife Sweden AB · Dec 2002