25 WATT CARBON DIOXIDE MEDICAL LASER FOR NEUROLOGY— 510(k) K864166

Name: FDA 510(k) clearance K864166
Creator: U.S. Food and Drug Administration
Published: 1987-02-10

Substantially Equivalent

Weck Surgical Systems

FDA 510(k) clearance K864166 for 25 WATT CARBON DIOXIDE MEDICAL LASER FOR NEUROLOGY, Substantially Equivalent on 1987-02-10. Applicant: Weck Surgical Systems. Device class: 3.

Clearance details

Applicant: Weck Surgical Systems
Product code: Code LKW
Device class: Class 3
Advisory panel: Unknown
Date received: 1986-10-23
Decision date: 1987-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hauppauge, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LKW

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K880172 — MODEL 4900 ND:YAG LASER FOR NEUROSURGERY APPLICA.1988-03-11
K853580 — MEDILAS 21986-02-13
K844440 — MODEL 4000 ND:YAG LASER FOR HEMORRHAGE CONTROL1985-05-09

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