LASER BENIGN & MALIGNANT PULMONARY OBSTRUCTIONS-— 510(k) K850432

Name: FDA 510(k) clearance K850432
Creator: U.S. Food and Drug Administration
Published: 1985-02-15

Substantially Equivalent

Cooper Lasersonics, Inc.

FDA 510(k) clearance K850432 for LASER BENIGN & MALIGNANT PULMONARY OBSTRUCTIONS-, Substantially Equivalent on 1985-02-15. Applicant: Cooper Lasersonics, Inc.. Device class: 2.

Clearance details

Applicant: Cooper Lasersonics, Inc.
Product code: Code LLO
Device class: Class 2
Regulation: 21 CFR 874.4500
Advisory panel: Ear, Nose, Throat
Date received: 1985-02-04
Decision date: 1985-02-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Clara, 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 Cooper Lasersonics, Inc.

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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.