Cleared Traditional

K820261 - MONITOR CO2 LASER SYSTEM

K820261 is the FDA 510(k) clearance for MONITOR CO2 LASER SYSTEM by Cooper Medical Corp.. It is a Class 2 Obstetrics & Gynecology device (product code HHR) cleared through the Traditional 510(k) pathway after a 31-day FDA review.

K820261 · Cooper Medical Corp. · Obstetrics & Gynecology device
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Mar 1982
Decision
31d
Days
Class 2
Risk

K820261 is an FDA 510(k) clearance for the MONITOR CO2 LASER SYSTEM. Classified as Laser, Surgical, Gynecologic (product code HHR), Class II - Special Controls.

Submitted by Cooper Medical Corp. (Walker, US). The FDA issued a Cleared decision on March 5, 1982 after a review of 31 days - a notably fast clearance cycle.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.4550 - the FDA obstetrics and gynecology 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 Cooper Medical Corp. devices

Submission Details

510(k) Number K820261 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 02, 1982
Decision Date March 05, 1982
Days to Decision 31 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
129d faster than avg
Panel avg: 160d · This submission: 31d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HHR Laser, Surgical, Gynecologic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.4550
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 Obstetrics & Gynecology devices follow this clearance model.

Regulatory Peers - HHR Laser, Surgical, Gynecologic

All 17
Devices cleared under the same product code (HHR) and FDA review panel - the closest regulatory comparables to K820261.
ND:YAG LASER 4000/6000/8000 ENDOMETRIAL ABLATION
K862456 · Cooper Lasersonics, Inc. · Aug 1986
MODEL 8-B WITH LA-2B ATTACHMENT FOR OB-GYN USE
K861845 · Directed Energy, Inc. · Aug 1986
CO2 LASER LAPAROSCOPE SYSTEM
K854361 · Richard Wolf Medical Instruments Corp. · Feb 1986
LASER, CO2 SURGICAL
K782054 · Cavitron Corp. · Jan 1979