SURGI-LIGHT ND:YAG LASER FOR UROLOGICAL USE— 510(k) K880071

Name: FDA 510(k) clearance K880071
Creator: U.S. Food and Drug Administration
Published: 1988-03-22

Substantially Equivalent

Laserguide

FDA 510(k) clearance K880071 for SURGI-LIGHT ND:YAG LASER FOR UROLOGICAL USE, Substantially Equivalent on 1988-03-22. Applicant: Laserguide. Device class: 2.

Clearance details

Applicant: Laserguide
Product code: Code FCS
Device class: Class 2
Regulation: 21 CFR 876.4020
Advisory panel: Gastroenterology, Urology
Date received: 1988-01-11
Decision date: 1988-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Barbara, CA, US

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More clearances from Laserguide

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K873892 — SURGI-LIGHT DISPOS.FIBEROPTIC DEL/SYS GI/URO USE1988-02-02
K875104 — SURGI-LIGHT DISPOSABLE SYSTEM FOR PULMONOLOGY 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.