PEREGRINE DIFFUSION LIGHT PIPE— 510(k) K950529

Name: FDA 510(k) clearance K950529
Creator: U.S. Food and Drug Administration
Published: 1995-06-07

Substantially Equivalent

Peregrine Surgical , Ltd.

FDA 510(k) clearance K950529 for PEREGRINE DIFFUSION LIGHT PIPE, Substantially Equivalent on 1995-06-07. Applicant: Peregrine Surgical , Ltd.. Device class: 2.

Clearance details

Applicant: Peregrine Surgical , Ltd.
Product code: Code HJM
Device class: Class 2
Regulation: 21 CFR 886.1945
Advisory panel: Ophthalmic
Date received: 1995-02-07
Decision date: 1995-06-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Doylestown, PA, 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.