Cleared Traditional

K801246 - OXFORD HUMAN MILK PASTEURISER

K801246 is the FDA 510(k) clearance for OXFORD HUMAN MILK PASTEURISER by Vickers America Medical Corp.. It is a Class 2 Obstetrics & Gynecology device (product code HGX) cleared through the Traditional 510(k) pathway after a 128-day FDA review.

K801246 · Vickers America Medical Corp. · Obstetrics & Gynecology device
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Oct 1980
Decision
128d
Days
Class 2
Risk

K801246 is an FDA 510(k) clearance for the OXFORD HUMAN MILK PASTEURISER. Classified as Pump, Breast, Powered (product code HGX), Class II - Special Controls.

Submitted by Vickers America Medical Corp. (Mchenry, US). The FDA issued a Cleared decision on October 3, 1980 after a review of 128 days - within the typical 510(k) review window.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.5160 - 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. Standard predicate reliance. 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 Vickers America Medical Corp. devices

Submission Details

510(k) Number K801246 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 28, 1980
Decision Date October 03, 1980
Days to Decision 128 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
32d faster than avg
Panel avg: 160d · This submission: 128d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HGX Pump, Breast, Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.5160
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.