IMAGENET DIGITAL OPHTHALMIC IMAGING SYSTEM— 510(k) K870039

Name: FDA 510(k) clearance K870039
Creator: U.S. Food and Drug Administration
Published: 1987-02-12

Substantially Equivalent

Par Microsystems Corp.

FDA 510(k) clearance K870039 for IMAGENET DIGITAL OPHTHALMIC IMAGING SYSTEM, Substantially Equivalent on 1987-02-12. Applicant: Par Microsystems Corp.. Device class: 1.

Clearance details

Applicant: Par Microsystems Corp.
Product code: Code DSF
Device class: Class 1
Regulation: 21 CFR 870.2810
Advisory panel: Cardiovascular
Date received: 1987-01-05
Decision date: 1987-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Hartford, NY, US

Download summary PDF View on FDA.gov ↗

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