VESSEL DILATOR— 510(k) K832595

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K832595 for VESSEL DILATOR, Substantially Equivalent on 1983-08-31. Applicant: Abbott Laboratories. Device class: 2.

Clearance details

Applicant: Abbott Laboratories
Product code: Code DWP
Device class: Class 2
Regulation: 21 CFR 870.4475
Advisory panel: Cardiovascular
Date received: 1983-08-02
Decision date: 1983-08-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Abbott Park, 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.