Cleared Traditional

E-Z CLEAR SMOKE EVACUATION ELECTROSURGICAL PENCIL;CLEAR NOZZLE EXTENTION, ULPA FILTER, CHARCOAL FILTER, ADAPTER

K141587 · Megadyne Medical Products, Inc. · General & Plastic Surgery
Feb 2015
Decision
250d
Days
Class 2
Risk

About This 510(k) Submission

K141587 is an FDA 510(k) clearance for the E-Z CLEAR SMOKE EVACUATION ELECTROSURGICAL PENCIL;CLEAR NOZZLE EXTENTION, ULPA FILTER, CHARCOAL FILTER, ADAPTER, a Electrosurgical, Cutting & Coagulation & Accessories (Class II — Special Controls, product code GEI), submitted by Megadyne Medical Products, Inc. (Draper, US). The FDA issued a Cleared decision on February 18, 2015, 250 days after receiving the submission on June 13, 2014. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4400.

Submission Details

510(k) Number K141587 FDA.gov
FDA Decision Cleared SESE
Date Received June 13, 2014
Decision Date February 18, 2015
Days to Decision 250 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code GEI — Electrosurgical, Cutting & Coagulation & Accessories
Device Class Class II — 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).

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