Cleared Traditional

K040788 - CALM PATTERNS, VERSION 01.00.00

K040788 is an FDA 510(k) clearance for CALM PATTERNS, manufactured by Lms Medical Systems , Ltd.. The device is a Class 2 Obstetrics & Gynecology device with product code HGM cleared through the Traditional 510(k) pathway after a 316-day FDA review.

K040788 · Lms Medical Systems , Ltd. · Obstetrics & Gynecology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 2005
Decision
316d
Days
Class 2
Risk

K040788 is an FDA 510(k) clearance for the CALM PATTERNS, VERSION 01.00.00. Classified as System, Monitoring, Perinatal (product code HGM), Class II - Special Controls.

Submitted by Lms Medical Systems , Ltd. (Montreal, Qc, CA). The FDA issued a Cleared decision on February 8, 2005 after a review of 316 days - an unusually long review period, suggesting complex equivalence evaluation.

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. Elevated predicate reliance profile. 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 Lms Medical Systems , Ltd. devices

FDA 510(k) Submission Details - K040788

510(k) Number K040788 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 29, 2004
Decision Date February 08, 2005
Days to Decision 316 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
156d slower than avg
Panel avg: 160d · This submission: 316d
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 141
Devices cleared under the same product code (HGM) and FDA review panel - the closest regulatory comparables to K040788.
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