Cleared Traditional

K926297 - REFLEX ESI

K926297 is the FDA 510(k) clearance for REFLEX ESI by Richard-Allan Medical Ind., Inc.. It is a Class 2 General & Plastic Surgery device (product code GEI) cleared through the Traditional 510(k) pathway after a 305-day FDA review.

K926297 · Richard-Allan Medical Ind., Inc. · General & Plastic Surgery device
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Oct 1993
Decision
305d
Days
Class 2
Risk

K926297 is an FDA 510(k) clearance for the REFLEX ESI. Classified as Electrosurgical, Cutting & Coagulation & Accessories within the GEI classification (a category for electrosurgical cutting and coagulation devices), Class II - Special Controls.

Submitted by Richard-Allan Medical Ind., Inc. (Richland, US). The FDA issued a Cleared decision on October 15, 1993 after a review of 305 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4400 - the FDA general and plastic surgery 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 General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Richard-Allan Medical Ind., Inc. devices

Submission Details

510(k) Number K926297 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 14, 1992
Decision Date October 15, 1993
Days to Decision 305 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
190d slower than avg
Panel avg: 115d · This submission: 305d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GEI Electrosurgical, Cutting & Coagulation & Accessories
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4400
Definition Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission If The Device Is Reusable And Has Specific Design Features (please Refer To Table 2 Of 82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).
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 General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - GEI Electrosurgical, Cutting & Coagulation & Accessories

All 1131
Devices cleared under the same product code (GEI) and FDA review panel - the closest regulatory comparables to K926297.
PILLING LAPAROSCOPIC INSTRUMENTATION
K934427 · Pilling Co. · Jan 1994
PHX TECHNOLOGIES CORP ELECTROSURGICAL PROBES
K932392 · Phx Technologies Corp. · Nov 1993
ORC ENDOSCOPIC MONOPOLAR ELECTROSURGICAL PROBE
K926242 · O.R. Concepts, Inc. · Oct 1993
TECH-SWITCH ELECTROSURGICAL PENCIL, REUSABLE
K932518 · Conmedcorp · Oct 1993
VALLEYLAB #E2751 & E2780R LAPAROSCOPIC HANDPIECE
K925647 · Valleylab, Inc. · Sep 1993
POLYP SNARE NET W/MONOPOLAR CAUTERY
K926103 · United States Endoscopy Group, Inc. · Sep 1993