DOSI FLOW— 510(k) K851058

Substantially Equivalent

Leventon, S.A.

FDA 510(k) clearance K851058 for DOSI FLOW, Substantially Equivalent on 1985-04-29. Applicant: Leventon, S.A.. Device class: 2.

Clearance details

Applicant: Leventon, S.A.
Product code: Code LDR
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1985-03-14
Decision date: 1985-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Barcelona, ES

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More clearances from Leventon, S.A.

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