STENTOR, PAGEVIEW— 510(k) K992698

Substantially Equivalent

Stentor, Inc.

FDA 510(k) clearance K992698 for STENTOR, PAGEVIEW, Substantially Equivalent on 1999-10-25. Applicant: Stentor, Inc.. Device class: 1.

Clearance details

Applicant: Stentor, Inc.
Product code: Code LMD
Device class: Class 1
Regulation: 21 CFR 892.2020
Advisory panel: Radiology
Date received: 1999-08-11
Decision date: 1999-10-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Leandro, 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.