Cleared Traditional

K983204 - HARWILL MEDICAL U-KLIP UMBILICAL CLAMP (FDA 510(k) Clearance)

Class II Obstetrics & Gynecology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K983204 · Harwill Medical (Pty) , Ltd. · Obstetrics & Gynecology device
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Feb 1999
Decision
165d
Days
Class 2
Risk

K983204 is an FDA 510(k) clearance for the HARWILL MEDICAL U-KLIP UMBILICAL CLAMP. Classified as Clamp, Umbilical (product code HFW), Class II - Special Controls.

Submitted by Harwill Medical (Pty) , Ltd. (Crofton, US). The FDA issued a Cleared decision on February 26, 1999 after a review of 165 days - an extended review cycle.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.4530 - 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 Harwill Medical (Pty) , Ltd. devices

Submission Details

510(k) Number K983204 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 14, 1998
Decision Date February 26, 1999
Days to Decision 165 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
5d slower than avg
Panel avg: 160d · This submission: 165d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HFW Clamp, Umbilical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.4530
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.