MODEL 4900 ND:YAG LASER FOR GASTRO & GENITOUR APPL— 510(k) K880171

Name: FDA 510(k) clearance K880171
Creator: U.S. Food and Drug Administration
Published: 1988-04-11

Substantially Equivalent

Cooper Lasersonics, Inc.

FDA 510(k) clearance K880171 for MODEL 4900 ND:YAG LASER FOR GASTRO & GENITOUR APPL, Substantially Equivalent on 1988-04-11. Applicant: Cooper Lasersonics, Inc.. Device class: 2.

Clearance details

Applicant: Cooper Lasersonics, Inc.
Product code: Code LNK
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 1988-01-15
Decision date: 1988-04-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Clara, CA, 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

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K880427 — ILLUMINA 40 CO2 LASER SYSTEM1988-04-18
K880428 — ILLUMINA 25 CO2 LASER SYSTEM1988-04-18
K880429 — ILLUMINA 55 CO2 LASER SYSTEM1988-04-18
K880807 — ILLUMINA MODEL 25 CO2 LASER FOR GENERAL/PLASTIC SU1988-04-18
K880808 — ILLUMINA MODEL 40 CO2 LASER FOR GENERAL/PLASTIC SU1988-04-18

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