DENSICOMP 250— 510(k) K904587

Substantially Equivalent

L. Keroack Co.

FDA 510(k) clearance K904587 for DENSICOMP 250, Substantially Equivalent on 1991-01-24. Applicant: L. Keroack Co.. Device class: 2.

Clearance details

Applicant: L. Keroack Co.
Product code: Code KPW
Device class: Class 2
Regulation: 21 CFR 892.1610
Advisory panel: Radiology
Date received: 1990-10-09
Decision date: 1991-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canada H3x 3p3, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code KPW

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Data sourced from openFDA. This site is unofficial and independent of the FDA.