Cleared Traditional

K051175 - CIV-OB OBSTRICAL MONITORING SOFTWARE APPLICATION

K051175 is an FDA 510(k) clearance for CIV-OB OBSTRICAL MONITORING SOFTWARE AP..., manufactured by Civent Communications, Ltd.. The device is a Class 2 Obstetrics & Gynecology device with product code HGM cleared through the Traditional 510(k) pathway after a 287-day FDA review.

K051175 · Civent Communications, Ltd. · Obstetrics & Gynecology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 2006
Decision
287d
Days
Class 2
Risk

K051175 is an FDA 510(k) clearance for the CIV-OB OBSTRICAL MONITORING SOFTWARE APPLICATION. Classified as System, Monitoring, Perinatal (product code HGM), Class II - Special Controls.

Submitted by Civent Communications, Ltd. (Moshav Hemed, IL). The FDA issued a Cleared decision on February 17, 2006 after a review of 287 days - an extended review cycle.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.2740 - 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 Civent Communications, Ltd. devices

FDA 510(k) Submission Details - K051175

510(k) Number K051175 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 06, 2005
Decision Date February 17, 2006
Days to Decision 287 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
127d slower than avg
Panel avg: 160d · This submission: 287d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HGM Device Classification - Class 2, Special Controls

Product Code HGM System, Monitoring, Perinatal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.2740
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 - HGM System, Monitoring, Perinatal

All 137
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