PEREGRINE WIDE ANGLE LIGHT PIPE— 510(k) K940393

Name: FDA 510(k) clearance K940393
Creator: U.S. Food and Drug Administration
Published: 1994-09-02

Substantially Equivalent

Peregrine Surgical , Ltd.

FDA 510(k) clearance K940393 for PEREGRINE WIDE ANGLE LIGHT PIPE, Substantially Equivalent on 1994-09-02. 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: 1994-01-26
Decision date: 1994-09-02
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.