Cleared Traditional

K953799 - DG EXAMINER PLUS

K953799 is an FDA 510(k) clearance for DG EXAMINER PLUS, manufactured by Medelec , Ltd.. The device is a Class 2 Neurology device with product code OLT cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K953799 · Medelec , Ltd. · Neurology device
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Nov 1995
Decision
86d
Days
Class 2
Risk

K953799 is an FDA 510(k) clearance for the DG EXAMINER PLUS. Classified as Non-normalizing Quantitative Electroencephalograph Software (product code OLT), Class II - Special Controls.

Submitted by Medelec , Ltd. (Old Woking, Surrey, DE). The FDA issued a Cleared decision on November 8, 1995 after a review of 86 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.1400 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Medelec , Ltd. devices

FDA 510(k) Submission Details - K953799

510(k) Number K953799 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 14, 1995
Decision Date November 08, 1995
Days to Decision 86 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
62d faster than avg
Panel avg: 148d · This submission: 86d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

OLT Device Classification - Class 2, Special Controls

Product Code OLT Non-normalizing Quantitative Electroencephalograph Software
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.1400
Definition Analyze Electroencephalograph Data Using Conventional Methodology To Output And Display Standard Electroencephalograph Parameters For Interpretation By A Qualified User.
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 - OLT Non-normalizing Quantitative Electroencephalograph Software

All 31
Devices cleared under the same product code (OLT) and FDA review panel - the closest regulatory comparables to K953799.
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