Laser Optical Catheter System

FDA 510(k) K880991 · Medline Industries, Inc.

Substantially Equivalent

510(k) numberK880991

Submission

Device name
Laser Optical Catheter System
Applicant
Medline Industries, Inc.
Englewood, CO, US
Received
March 8, 1988
Decision date
May 25, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HHR – Laser, Surgical, Gynecologic
Device class
Class II (moderate risk)
Regulation
21 CFR 884.4550
Specialty
Obstetrics/Gynecology

Other 510(k)s with product code HHR

510(k)DeviceApplicantDecision
K881507Endocoagulator Model 20 Laser & AccessoriesHHR · Traditional Hgm Medical Laser Systems, Inc.04/27/1989SE
K871875Model 5050 Surgilaser for Ob-Gyn UseHHR · Traditional Lasermatic, Inc.08/22/1988SE
K875314GL-35 Colposcopic Laser SystemHHR · Traditional Laser Engineering, Inc.08/05/1988SE
K874615Laser Cannister FilterHHR · Traditional Medical Marketing, Inc.06/23/1988SE
K880591Laseguide 600A, 600B, 400A, 400B for Ob-Gyn UseHHR · Traditional Laser Peripherals, LLC06/01/1988SE
K880930MDLS 4000,4900,6000,8000,8900 ND:YAG/1700 C02 LaseHHR · Traditional Copper Lasersonics, Inc.05/31/1988SE
K880173Model 4900 Nd:Yag Laser for Endometrial AblationHHR · Traditional Cooper Lasersonics, Inc.03/24/1988SE
K874837KTP/532 Laser for Ob-Gyn UseHHR · Traditional Laserscope03/14/1988SE
K875078Heracure LS 500HHR · Traditional W.C. Heraeus GmbH02/22/1988SE
K872709Model 20-C, RL-20A/U, OB-10A/UHHR · Traditional Directed Energy, Inc.02/02/1988SE

More from Directed Energy, Inc.

510(k)DeviceDecision
K253526NAMIC Dilator and SheathDYB · Traditional 07/29/2026SE
K254287Medline Reusable Blood Pressure CuffDXQ · Traditional 06/22/2026SE
K253322Hudson RCI® Infant Dri-TechTM Breathing Circuits (HUD99060 / Dri-Tech with 78” Infant…BZE · Traditional 03/25/2026SE
K251687Konig Bell Circumcision ClampHFX · Traditional 02/25/2026SE
K253070Namic Radial Arm Band, 23 cm (DYNJRADBAND); Namic Radial Arm Band, 26 cm (DYNJRADBANDL)DXC · Traditional 11/20/2025SE
K250345Medline Bag DecanterLHI · Traditional 10/24/2025SE
K250312Hudson RCI® Comfort Flo Nasal Cannula Premature, Infant; Hudson RCI® Comfort Flo Plus…BTT · Traditional 07/02/2025SE
K243888Medline UNITE® REFLEX® Hybrid Nitinol Implant SystemJDR · Traditional 04/11/2025SE
K242844Medline Level 4 Surgical Gown with Breathable SleevesFYA · Traditional 02/26/2025SE
K242370Medline Microdissection Needle (4cm) (140936 (ESE104A)); Medline Microdissection Needle…GEI · Traditional 12/19/2024SE

Questions and answers

When was Laser Optical Catheter System cleared by the FDA?

Laser Optical Catheter System (K880991) received a 510(k) decision of Substantially Equivalent on May 25, 1988, 78 days after the submission was received.

What is the product code of K880991?

The FDA product code is HHR – Laser, Surgical, Gynecologic, a Class II (moderate risk) device regulated under 21 CFR 884.4550.