Cleared Traditional

K951897 - POWER RESECTOSCOPE CUTTING LOOP

K951897 is an FDA 510(k) clearance for POWER RESECTOSCOPE CUTTING LOOP, manufactured by Power Analytics Corp.. The device is a Class 2 Gastroenterology & Urology device with product code FAS cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K951897 · Power Analytics Corp. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1995
Decision
85d
Days
Class 2
Risk

K951897 is an FDA 510(k) clearance for the POWER RESECTOSCOPE CUTTING LOOP. Classified as Electrode, Electrosurgical, Active, Urological (product code FAS), Class II - Special Controls.

Submitted by Power Analytics Corp. (Sacramento, US). The FDA issued a Cleared decision on July 18, 1995 after a review of 85 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.4300 - the FDA gastroenterology and urology 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 Power Analytics Corp. devices

FDA 510(k) Submission Details - K951897

510(k) Number K951897 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 24, 1995
Decision Date July 18, 1995
Days to Decision 85 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
45d faster than avg
Panel avg: 130d · This submission: 85d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FAS Device Classification - Class 2, Special Controls

Product Code FAS Electrode, Electrosurgical, Active, Urological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.4300
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 Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - FAS Electrode, Electrosurgical, Active, Urological

All 29
Devices cleared under the same product code (FAS) and FDA review panel - the closest regulatory comparables to K951897.
ARTHROCARE BIPOLAR LOOP ELECTRODE SYSTEM
K955531 · Arthrocare Corp. · Feb 1996
SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES
K953453 · Symbiosis Corp. · Jan 1996
ROLLER ELECTRODE
K951863 · Olympus America, Inc. · Aug 1995
KARL STORZ UNIPOLAR BALL, NEEDLE, LOOP ELECTRODES
K944795 · KARL STORZ Endoscopy-America, Inc. · Dec 1994
HF-RESECTION ELECTRODE, LOOP W/RUNNER ENDOS/ACCESS
K931763 · Olympus Corp. · Aug 1994