SINUSCAN 102/SINUSPRINT— 510(k) K960421

Substantially Equivalent

Ferguson Medical

FDA 510(k) clearance K960421 for SINUSCAN 102/SINUSPRINT, Substantially Equivalent on 1997-04-16. Applicant: Ferguson Medical. Device class: 2.

Clearance details

Applicant: Ferguson Medical
Product code: Code LWI
Device class: Class 2
Regulation: 21 CFR 892.1560
Advisory panel: Radiology
Date received: 1996-01-29
Decision date: 1997-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chico, CA, 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.