Cleared Traditional

K823924 - MODEL SSE4 ELECTROSURGICAL GENERATOR

K823924 is an FDA 510(k) clearance for MODEL SSE4 ELECTROSURGICAL GENERATOR, manufactured by Valleylab, Inc.. The device is a Class 2 General & Plastic Surgery device with product code GEI cleared through the Traditional 510(k) pathway after a 12-day FDA review.

K823924 · Valleylab, Inc. · General & Plastic Surgery device
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Jan 1983
Decision
12d
Days
Class 2
Risk

K823924 is an FDA 510(k) clearance for the MODEL SSE4 ELECTROSURGICAL GENERATOR. Classified as Electrosurgical, Cutting & Coagulation & Accessories within the GEI classification (a category for electrosurgical cutting and coagulation devices), Class II - Special Controls.

Submitted by Valleylab, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 9, 1983 after a review of 12 days - a notably fast clearance cycle.

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: 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 Valleylab, Inc. devices

FDA 510(k) Submission Details - K823924

510(k) Number K823924 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 28, 1982
Decision Date January 09, 1983
Days to Decision 12 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
103d faster than avg
Panel avg: 115d · This submission: 12d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GEI Device Classification - Class 2, Special Controls

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 1192
Devices cleared under the same product code (GEI) and FDA review panel - the closest regulatory comparables to K823924.
DISPERSIVE ELECTRODE
K830545 · C.R. Bard, Inc. · Mar 1983
MF 360B ELECTROSURGICAL UNIT
K823923 · Aspen Laboratories, Inc. · Feb 1983
3M SCOTCHPLATE 51148 SMALL CONDUCTIVE
K823689 · 3M Company · Jan 1983
ELECTROSURGICAL UNIT
K823083 · Kelleher Corp. · Dec 1982
BIPOLAR COAGULATOR #9620/9621
K823184 · Concept, Inc. · Dec 1982
DISP. METAL & PLASTIC ELECTROSURG. DEV
K822355 · Valleylab, Inc. · Sep 1982