Cleared Traditional

K950406 - DEVICE

K950406 is the FDA 510(k) clearance for DEVICE by Aaron Medical Industries. It is a Class 2 General & Plastic Surgery device (product code GEI) cleared through the Traditional 510(k) pathway after a 72-day FDA review.

K950406 · Aaron Medical Industries · General & Plastic Surgery device
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Apr 1995
Decision
72d
Days
Class 2
Risk

K950406 is an FDA 510(k) clearance for the DEVICE, ELECTROSURGICAL, CUTTING AND COAGULATION & ACCESSORIES. Classified as Electrosurgical, Cutting & Coagulation & Accessories within the GEI classification (a category for electrosurgical cutting and coagulation devices), Class II - Special Controls.

Submitted by Aaron Medical Industries (St. Petersburg, US). The FDA issued a Cleared decision on April 13, 1995 after a review of 72 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 Aaron Medical Industries devices

Submission Details

510(k) Number K950406 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 31, 1995
Decision Date April 13, 1995
Days to Decision 72 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
43d faster than avg
Panel avg: 115d · This submission: 72d
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 1137
Devices cleared under the same product code (GEI) and FDA review panel - the closest regulatory comparables to K950406.
CONMED/ASPEN LABS COATED LAPAROSCOPIC ELECTROSURGICAL BLADES
K952204 · Conmedcorp · May 1995
MANUAL SURGICAL INSRUMENT
K951589 · United States Surgical, A Division of Tyco Healthc · May 1995
HI-TIP HIGH TEMPERATURE REPLACEMENT TIP
K945758 · Aaron Medical Industries · Apr 1995
BIPOLAR FORCEPS
K951035 · Megadyne Medical Products, Inc. · Apr 1995
FINESS I (DERMATOLOGIC APPLICATION)
K951032 · Utah Medical Products, Inc. · Apr 1995
SMOKIEVAC ELECTROSURGICAL PENCIL
K946104 · Aspen Laboratories, Inc. · Apr 1995