Cleared Traditional

K052692 - SURETEK MEDICAL REPROCESSED ELECTROSURGICAL ELECTRODES

K052692 is an FDA 510(k) clearance for SURETEK MEDICAL REPROCESSED ELECTROSURG..., manufactured by Suretek Medical. The device is a Class 2 General & Plastic Surgery device with product code NUJ cleared through the Traditional 510(k) pathway after a 224-day FDA review.

K052692 · Suretek Medical · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2006
Decision
224d
Days
Class 2
Risk

K052692 is an FDA 510(k) clearance for the SURETEK MEDICAL REPROCESSED ELECTROSURGICAL ELECTRODES. Classified as Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed (product code NUJ), Class II - Special Controls.

Submitted by Suretek Medical (Greenville, US). The FDA issued a Cleared decision on May 10, 2006 after a review of 224 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. 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 Suretek Medical devices

FDA 510(k) Submission Details - K052692

510(k) Number K052692 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 28, 2005
Decision Date May 10, 2006
Days to Decision 224 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
109d slower than avg
Panel avg: 115d · This submission: 224d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

NUJ Device Classification - Class 2, Special Controls

Product Code NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4400
Definition Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission. (70 Fr 56911, Available At Https://www.govinfo.gov/content/pkg/fr-2005-09-29/pdf/05-19510.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 - NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

All 30
Devices cleared under the same product code (NUJ) and FDA review panel - the closest regulatory comparables to K052692.
REPROCESSED HAND ACTIVATE SEALER/DIVIDER
K111600 · Ascent Healthcare Solutions · Nov 2011
REPROCESSED ELECTROSURGICAL INSTRUMENT
K110189 · Ascent Healthcare Solutions · Jul 2011
REPROCESSED SCISSOR TIPS
K073613 · Sterilmed, Inc. · Feb 2008
VANGUARD REPROCESSED ARTHROSCOPIC WANDS
K043198 · Vanguard Medical Concepts, Inc. · May 2005
REPROCESSED LAPAROSCOPIC ELECTRIC INSTUMENTS
K012598 · Sterilmed, Inc. · Nov 2001
REPROCESSED AUTOSUTURE UNIPOLAR LAPAROSCOPIC/ENDOSCOPIC INSTRUMENTS
K012603 · Alliance Medical Corp. · Nov 2001