CLEARVIEW— 510(k) K790536

Substantially Equivalent

Hipoint Research, Inc.

FDA 510(k) clearance K790536 for CLEARVIEW, Substantially Equivalent on 1979-03-28. Applicant: Hipoint Research, Inc.. Device class: 2.

Clearance details

Applicant: Hipoint Research, Inc.
Product code: Code KXJ
Device class: Class 2
Regulation: 21 CFR 892.1980
Advisory panel: Radiology
Date received: 1979-03-22
Decision date: 1979-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.