SURGI-LIGHT DISPOS.FIBEROPTIC DEL/SYS GI/URO USE— 510(k) K873892

Substantially Equivalent

Laserguide

FDA 510(k) clearance K873892 for SURGI-LIGHT DISPOS.FIBEROPTIC DEL/SYS GI/URO USE, Substantially Equivalent on 1988-02-02. Applicant: Laserguide.

Clearance details

Applicant
Laserguide
Product code
Code LNK
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Santa Barbara, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.