FILMFAX— 510(k) K895209

Substantially Equivalent

Discovery Systems, Inc.

FDA 510(k) clearance K895209 for FILMFAX, Substantially Equivalent on 1989-10-27. Applicant: Discovery Systems, Inc.. Device class: 1.

Clearance details

Applicant: Discovery Systems, Inc.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1989-08-17
Decision date: 1989-10-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Overland Park, KS, 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.