FIBERLASE II ND:YAG LASER FOR PULMONARY USE— 510(k) K872351

Name: FDA 510(k) clearance K872351
Creator: U.S. Food and Drug Administration
Published: 1987-12-11

Substantially Equivalent

Laser Media

FDA 510(k) clearance K872351 for FIBERLASE II ND:YAG LASER FOR PULMONARY USE, Substantially Equivalent on 1987-12-11. Applicant: Laser Media. Device class: 2.

Clearance details

Applicant: Laser Media
Product code: Code LLO
Device class: Class 2
Regulation: 21 CFR 874.4500
Advisory panel: Ear, Nose, Throat
Date received: 1987-06-17
Decision date: 1987-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hauppauge, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LLO

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K884815 — SLT CLMD CONTACT LASER1988-12-22
K881499 — SURGILASE YAG 100 FOR GYNECOLOGY USE1988-04-29
K880592 — LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE1988-04-25
K880170 — MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS1988-03-24
K874254 — ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS1988-03-04

More clearances from Laser Media

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K872352 — FIBERLASE II ND:YAG LASER FOR TREAT OF MENORRHAGIA1987-12-30
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.