PUPIL PATHWAY ANALYZER (PPA)— 510(k) K895609

Name: FDA 510(k) clearance K895609
Creator: U.S. Food and Drug Administration
Published: 1989-11-02

Substantially Equivalent

Pulse Medical Instruments

FDA 510(k) clearance K895609 for PUPIL PATHWAY ANALYZER (PPA), Substantially Equivalent on 1989-11-02. Applicant: Pulse Medical Instruments. Device class: 1.

Clearance details

Applicant: Pulse Medical Instruments
Product code: Code HLG
Device class: Class 1
Regulation: 21 CFR 886.1700
Advisory panel: Ophthalmic
Date received: 1989-09-18
Decision date: 1989-11-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Costa Mesa, CA, US

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