LASEGUIDE 600A, 600B, 400A, AND 400B— 510(k) K874680

Name: FDA 510(k) clearance K874680
Creator: U.S. Food and Drug Administration
Published: 1988-03-23

Substantially Equivalent

Laser Peripherals, LLC

FDA 510(k) clearance K874680 for LASEGUIDE 600A, 600B, 400A, AND 400B, Substantially Equivalent on 1988-03-23. Applicant: Laser Peripherals, LLC. Device class: 2.

Clearance details

Applicant: Laser Peripherals, LLC
Product code: Code FCS
Device class: Class 2
Regulation: 21 CFR 876.4020
Advisory panel: Gastroenterology, Urology
Date received: 1987-11-13
Decision date: 1988-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hingham, MA, US

Download summary PDF View on FDA.gov ↗

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