Cleared Traditional

K031427 - ELECTRO NEUROMUSCULAR STIMULATOR, MODEL BMLS03-1

K031427 is an FDA 510(k) clearance for ELECTRO NEUROMUSCULAR STIMULATOR, manufactured by Biomedical Life Systems, Inc.. The device is a Class 2 Physical Medicine device with product code IPF cleared through the Traditional 510(k) pathway after a 105-day FDA review.

K031427 · Biomedical Life Systems, Inc. · Physical Medicine device
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Aug 2003
Decision
105d
Days
Class 2
Risk

K031427 is an FDA 510(k) clearance for the ELECTRO NEUROMUSCULAR STIMULATOR, MODEL BMLS03-1. Classified as Stimulator, Muscle, Powered (product code IPF), Class II - Special Controls.

Submitted by Biomedical Life Systems, Inc. (Vista, US). The FDA issued a Cleared decision on August 19, 2003 after a review of 105 days - within the typical 510(k) review window.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5850 - the FDA physical medicine 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 Physical Medicine review framework, consistent with the majority of Class II 510(k) submissions.

View all Biomedical Life Systems, Inc. devices

FDA 510(k) Submission Details - K031427

510(k) Number K031427 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 06, 2003
Decision Date August 19, 2003
Days to Decision 105 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
11d faster than avg
Panel avg: 116d · This submission: 105d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IPF Device Classification - Class 2, Special Controls

Product Code IPF Stimulator, Muscle, Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.5850
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 Physical Medicine devices follow this clearance model.

Regulatory Peers - IPF Stimulator, Muscle, Powered

All 355
Devices cleared under the same product code (IPF) and FDA review panel - the closest regulatory comparables to K031427.
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