ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS— 510(k) K874254

Name: FDA 510(k) clearance K874254
Creator: U.S. Food and Drug Administration
Published: 1988-03-04

Substantially Equivalent

Minnesota Laser Corp.

FDA 510(k) clearance K874254 for ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONS, Substantially Equivalent on 1988-03-04. Applicant: Minnesota Laser Corp.. Device class: 2.

Clearance details

Applicant: Minnesota Laser Corp.
Product code: Code LLO
Device class: Class 2
Regulation: 21 CFR 874.4500
Advisory panel: Ear, Nose, Throat
Date received: 1987-10-20
Decision date: 1988-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Roseville, MN, 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
K875104 — SURGI-LIGHT DISPOSABLE SYSTEM FOR PULMONOLOGY USE1988-02-02

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