Cleared Traditional

K932299 - ELECTRO-MESH

K932299 is the FDA 510(k) clearance for ELECTRO-MESH by Prizm Medical, Inc.. It is a Class 2 Neurology device (product code GXY) cleared through the Traditional 510(k) pathway after a 416-day FDA review.

K932299 · Prizm Medical, Inc. · Neurology device
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Jul 1994
Decision
416d
Days
Class 2
Risk

K932299 is an FDA 510(k) clearance for the ELECTRO-MESH. Classified as Electrode, Cutaneous (product code GXY), Class II - Special Controls.

Submitted by Prizm Medical, Inc. (Norcross, US). The FDA issued a Cleared decision on July 1, 1994 after a review of 416 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.1320 - the FDA neurology 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Neurology submissions.

View all Prizm Medical, Inc. devices

Submission Details

510(k) Number K932299 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 11, 1993
Decision Date July 01, 1994
Days to Decision 416 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
268d slower than avg
Panel avg: 148d · This submission: 416d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GXY Electrode, Cutaneous
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.1320
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 Neurology devices follow this clearance model.

Regulatory Peers - GXY Electrode, Cutaneous

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