Cleared Traditional

CLEANCUT (K972335) - FDA 510(k) Clearance

Class II General & Plastic Surgery device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K972335 · Medquest Products, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 1999
Decision
563d
Days
Class 2
Risk

K972335 is an FDA 510(k) clearance for the CLEANCUT. Classified as Electrosurgical, Cutting & Coagulation & Accessories within the GEI classification (a category for electrosurgical cutting and coagulation devices), Class II - Special Controls.

Submitted by Medquest Products, Inc. (Salt Lake City, US). The FDA issued a Cleared decision on January 7, 1999 after a review of 563 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind General & Plastic Surgery submissions.

View all Medquest Products, Inc. devices

Submission Details

510(k) Number K972335 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 23, 1997
Decision Date January 07, 1999
Days to Decision 563 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
448d slower than avg
Panel avg: 115d · This submission: 563d
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 571
Devices cleared under the same product code (GEI) and FDA review panel - the closest regulatory comparables to K972335.
DYONICS VARICOSE VEIN ABLATION BLADE
K990723 · Smith & Nephew, Inc. · Oct 1999
DEXIDE BIPOLAR FORCEPS II** DEVICE
K993055 · United States Surgical, A Division of Tyco Healthc · Oct 1999
DEXIDE BIPOLAR FORCEPS II ** DEVICE
K991859 · United States Surgical, A Division of Tyco Healthc · Jun 1999
ELECTROSURGICAL UNIT (ESU) (115 VOLT) MODEL 4810, ELECTROSURGICAL UNIT (ESU) (230 VOLT) MODEL 4811, INSTRUMENT CABLE, 19
K981981 · Boston Scientific Corp · Sep 1998
POWERSTAR BIPOLAR SCISSORS
K981361 · Ethicon, Inc. · Jul 1998
ETHICON NON-STICK BIPOLAR FORCEPS
K973384 · Ethicon, Inc. · Dec 1997