Cleared Traditional

K862444 - FIBERLASE 100 MEDICAL LASER SYS/ND:YAG MENORRHAGIA

K862444 is an FDA 510(k) clearance for FIBERLASE 100 MEDICAL LASER SYS/ND:YAG ..., manufactured by Laser Media. The device is a Class 2 Obstetrics & Gynecology device with product code HHR cleared through the Traditional 510(k) pathway after a 91-day FDA review.

K862444 · Laser Media · Obstetrics & Gynecology device
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Sep 1986
Decision
91d
Days
Class 2
Risk

K862444 is an FDA 510(k) clearance for the FIBERLASE 100 MEDICAL LASER SYS/ND:YAG MENORRHAGIA. Classified as Laser, Surgical, Gynecologic (product code HHR), Class II - Special Controls.

Submitted by Laser Media (Hauppauge, US). The FDA issued a Cleared decision on September 25, 1986 after a review of 91 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Obstetrics & Gynecology review framework, consistent with the majority of Class II 510(k) submissions.

View all Laser Media devices

FDA 510(k) Submission Details - K862444

510(k) Number K862444 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 26, 1986
Decision Date September 25, 1986
Days to Decision 91 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
69d faster than avg
Panel avg: 160d · This submission: 91d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HHR Device Classification - Class 2, Special Controls

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 24
Devices cleared under the same product code (HHR) and FDA review panel - the closest regulatory comparables to K862444.
OMNIPLUS PHOTOSURGICAL LASER SYSTEM FOR OB-GYN
K863221 · Laserscope · Mar 1987
MODEL 8900 ND:YAG LASER, TREATMENT OF MENORRHAGIA
K863361 · Cooper Lasersonics, Inc. · Nov 1986
SURGICAL CARBON DIOXIDE SYS. MODEL 10-C OB-GYN USE
K862861 · Directed Energy, Inc. · Oct 1986
CABOT LASER LAPAROSCOPY ACCESSORY SET
K862228 · Cabot Medical Corp. · Aug 1986
MODEL 8 & 20 ARGON LASER FOR PELVIC SURGERY IN GYN
K862227 · Hgm, Inc. · Aug 1986
ND:YAG LASER 4000/6000/8000 ENDOMETRIAL ABLATION
K862456 · Cooper Lasersonics, Inc. · Aug 1986