ANGIOTEC SC 1221 SCAN CONVERTER— 510(k) K850330

Substantially Equivalent

Angiotec

FDA 510(k) clearance K850330 for ANGIOTEC SC 1221 SCAN CONVERTER, Substantially Equivalent on 1985-04-30. Applicant: Angiotec. Device class: 2.

Clearance details

Applicant: Angiotec
Product code: Code LMA
Device class: Class 2
Regulation: 21 CFR 892.2030
Advisory panel: Radiology
Date received: 1985-01-28
Decision date: 1985-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burlingame, 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.