FIBERLASE II ND:YAG LASER FOR TREAT OF MENORRHAGIA— 510(k) K872352

Name: FDA 510(k) clearance K872352
Creator: U.S. Food and Drug Administration
Published: 1987-12-30

Substantially Equivalent

Laser Media

FDA 510(k) clearance K872352 for FIBERLASE II ND:YAG LASER FOR TREAT OF MENORRHAGIA, Substantially Equivalent on 1987-12-30. Applicant: Laser Media. Device class: 2.

Clearance details

Applicant: Laser Media
Product code: Code HHR
Device class: Class 2
Regulation: 21 CFR 884.4550
Advisory panel: Obstetrics/Gynecology
Date received: 1987-06-17
Decision date: 1987-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hauppauge, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HHR

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K881507 — ENDOCOAGULATOR MODEL 20 LASER & ACCESSORIES1989-04-27
K871875 — MODEL 5050 SURGILASER FOR OB-GYN USE1988-08-22
K875314 — GL-35 COLPOSCOPIC LASER SYSTEM1988-08-05
K874615 — LASER CANNISTER FILTER1988-06-23
K880591 — LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USE1988-06-01

More clearances from Laser Media

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K872351 — FIBERLASE II ND:YAG LASER FOR PULMONARY USE1987-12-11
K872350 — FIBERLASE II ND:YAG LASER FOR GASTRO.&UROLOGY USE1987-08-10
K872031 — UNI-FIBER NON-REPAIRABLE FIBER DELIVERY SYSTEM1987-08-04
K863428 — SINGLE USE LASER FIBER DELIVERY SYSTEM FOR ND: YAG1986-12-03
K863583 — CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASER1986-11-24

Data sourced from openFDA. This site is unofficial and independent of the FDA.