SURGI-LIGHT DISPOSABLE SYSTEM FOR PULMONOLOGY USE— 510(k) K875104

Name: FDA 510(k) clearance K875104
Creator: U.S. Food and Drug Administration
Published: 1988-02-02

Substantially Equivalent

Laserguide

FDA 510(k) clearance K875104 for SURGI-LIGHT DISPOSABLE SYSTEM FOR PULMONOLOGY USE, Substantially Equivalent on 1988-02-02. Applicant: Laserguide. Device class: 2.

Clearance details

Applicant: Laserguide
Product code: Code LLO
Device class: Class 2
Regulation: 21 CFR 874.4500
Advisory panel: Ear, Nose, Throat
Date received: 1987-12-18
Decision date: 1988-02-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Barbara, CA, 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 Laserguide

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K880071 — SURGI-LIGHT ND:YAG LASER FOR UROLOGICAL USE1988-03-22
K873892 — SURGI-LIGHT DISPOS.FIBEROPTIC DEL/SYS GI/URO USE1988-02-02
K873571 — LIGHT-TOUCH FIBEROPTIC MICROCONTACT PROBE1987-11-06
K873664 — LIGHT-SPOT FIBEROPTIC LASER HANDPIECE1987-11-06

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