PRIMUS MODEL CLC 330— 510(k) K891235

Substantially Equivalent

Primus, Inc.

FDA 510(k) clearance K891235 for PRIMUS MODEL CLC 330, Substantially Equivalent on 1989-06-16. Applicant: Primus, Inc.. Device class: 2.

Clearance details

Applicant: Primus, Inc.
Product code: Code LCP
Device class: Class 2
Regulation: 21 CFR 864.7470
Advisory panel: Hematology
Date received: 1989-03-07
Decision date: 1989-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kansas City, MO, 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.