MODEL 5050 SURGILASER FOR PULMONARY USE— 510(k) K871876

Name: FDA 510(k) clearance K871876
Creator: U.S. Food and Drug Administration
Published: 1988-01-22

Substantially Equivalent

Lasermatic, Inc.

FDA 510(k) clearance K871876 for MODEL 5050 SURGILASER FOR PULMONARY USE, Substantially Equivalent on 1988-01-22. Applicant: Lasermatic, Inc.. Device class: 2.

Clearance details

Applicant: Lasermatic, Inc.
Product code: Code LLO
Device class: Class 2
Regulation: 21 CFR 874.4500
Advisory panel: Ear, Nose, Throat
Date received: 1987-05-14
Decision date: 1988-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, 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 Lasermatic, Inc.

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K903131 — LASERMATIC SUPERCOMBO(TM) SURGICAL LASER SYSTEM1991-02-19
K901638 — MODIFIED COMBOLASER 5050 & NEW MODEL 5050 VER. 331990-06-27
K893529 — COMBOLASER MODEL 50501989-06-08
K871875 — MODEL 5050 SURGILASER FOR OB-GYN USE1988-08-22
K871932 — MODEL 5050 SURGILASER FOR UROLOGY USE1988-03-25

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