Model 8900 Nd:Yag Laser, Treatment of Menorrhagia

FDA 510(k) K863361 · Cooper Lasersonics, Inc.

Substantially Equivalent

510(k) numberK863361

Submission

Device name
Model 8900 Nd:Yag Laser, Treatment of Menorrhagia
Applicant
Cooper Lasersonics, Inc.
Santa Clara, CA, US
Received
September 2, 1986
Decision date
November 24, 1986
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
K880991Laser Optical Catheter SystemHHR · Traditional Medline Industries, Inc.05/25/1988SE
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

More from W.C. Heraeus GmbH

510(k)DeviceDecision
K880809Illumina Model 55 CO2 Laser for General/Plastic SuGEX · Traditional 04/18/1988SE
K880808Illumina Model 40 CO2 Laser for General/Plastic SuGEX · Traditional 04/18/1988SE
K880807Illumina Model 25 CO2 Laser for General/Plastic SuGEX · Traditional 04/18/1988SE
K880429Illumina 55 CO2 Laser SystemEWG · Traditional 04/18/1988SE
K880428Illumina 25 CO2 Laser SystemEWG · Traditional 04/18/1988SE
K880427Illumina 40 CO2 Laser SystemEWG · Traditional 04/18/1988SE
K880171Model 4900 Nd:Yag Laser for Gastro & Genitour ApplLNK · Traditional 04/11/1988SE
K880173Model 4900 Nd:Yag Laser for Endometrial AblationHHR · Traditional 03/24/1988SE
K880170Model 4900 Nd:Yag Laser for Pulmonary ObstructionsLLO · Traditional 03/24/1988SE
K880172Model 4900 Nd:Yag Laser for Neurosurgery Applica.LKW · Traditional 03/11/1988SE

Questions and answers

When was Model 8900 Nd:Yag Laser, Treatment of Menorrhagia cleared by the FDA?

Model 8900 Nd:Yag Laser, Treatment of Menorrhagia (K863361) received a 510(k) decision of Substantially Equivalent on November 24, 1986, 83 days after the submission was received.

What is the product code of K863361?

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