ND:YAG 100 SURGICAL LASER FOR NEURO & PULMONARY— 510(k) K875042

Name: FDA 510(k) clearance K875042
Creator: U.S. Food and Drug Administration
Published: 1988-06-24

Substantially Equivalent

Surgilase, Inc.

FDA 510(k) clearance K875042 for ND:YAG 100 SURGICAL LASER FOR NEURO & PULMONARY, Substantially Equivalent on 1988-06-24. Applicant: Surgilase, Inc.. Device class: 3.

Clearance details

Applicant: Surgilase, Inc.
Product code: Code LKW
Device class: Class 3
Advisory panel: Unknown
Date received: 1987-12-07
Decision date: 1988-06-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warwick, RI, 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
K864166 — 25 WATT CARBON DIOXIDE MEDICAL LASER FOR NEUROLOGY1987-02-10
K853580 — MEDILAS 21986-02-13
K844440 — MODEL 4000 ND:YAG LASER FOR HEMORRHAGE CONTROL1985-05-09

More clearances from Surgilase, Inc.

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K932421 — SURGILASE/OP 15, 20, 25, 30, 40, 50 CO2 SURG. LASE1993-10-15
K924664 — SURGILASE FIBERLASE CO2 LASER WAVEGUIDE1993-04-15
K905006 — SURGILASE SL 150 SURGICAL LASER SYSTEM1991-02-21
K904203 — SURGILASE SL 50/60 GOLD SURGICAL LASER SYSTEM1990-12-07
K902211 — SURGILASE YAG 100 SURGICAL LASER SYSTEM1990-06-29

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