ENDO-LASE CD-100 CO2 LASER FOR OTORHINOLARYNGOLOGY— 510(k) K853875

Name: FDA 510(k) clearance K853875
Creator: U.S. Food and Drug Administration
Published: 1986-01-09

Substantially Equivalent

Endo Lase, Inc.

FDA 510(k) clearance K853875 for ENDO-LASE CD-100 CO2 LASER FOR OTORHINOLARYNGOLOGY, Substantially Equivalent on 1986-01-09. Applicant: Endo Lase, Inc.. Device class: 2.

Clearance details

Applicant: Endo Lase, Inc.
Product code: Code EWG
Device class: Class 2
Regulation: 21 CFR 874.4500
Advisory panel: Ear, Nose, Throat
Date received: 1985-09-17
Decision date: 1986-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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K924652 — BENSON CCA1001993-04-09
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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

More clearances from Endo Lase, Inc.

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K853900 — ENDO-LASE CD40 FOR NEUROSURGERY1986-06-18
K853878 — ENDO-LASE CD-100 CO2 LASER FOR NEUROSURGERY1986-05-02
K853876 — ENDO-LSE CD-100 CO2 LASER FOR GYNECOLOGY1986-02-21
K853903 — ENDO-LASE CD40 CO2 FOR GYNECOLOGY1986-02-21
K855093 — MEDILAS 2 ND:YAG LASER SURGERY SYSTEM1986-02-21

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