MODEL 5050 SURGILASER FOR GASTRO-INTESTINAL USE— 510(k) K871934

Name: FDA 510(k) clearance K871934
Creator: U.S. Food and Drug Administration
Published: 1988-03-25

Substantially Equivalent

Lasermatic, Inc.

FDA 510(k) clearance K871934 for MODEL 5050 SURGILASER FOR GASTRO-INTESTINAL USE, Substantially Equivalent on 1988-03-25. Applicant: Lasermatic, Inc.. Device class: 2.

Clearance details

Applicant: Lasermatic, Inc.
Product code: Code LNK
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 1987-05-19
Decision date: 1988-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LNK

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K925395 — TECHNOMED PULSOLITH 4000 LASER SYSTEM1993-05-21
K901723 — MDL-2000 LASERTRIPTER1990-07-13
K874253 — ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA.1988-07-12
K874255 — ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI.1988-07-12
K880193 — MODEL 4060 N ND:YAG LASER FOR UROLOGICAL USE1988-04-14

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.