CORDOT R— 510(k) K854618

Substantially Equivalent

Cordis Corp.

FDA 510(k) clearance K854618 for CORDOT R, Substantially Equivalent on 1986-05-01. Applicant: Cordis Corp.. Device class: 2.

Clearance details

Applicant
Cordis Corp.
Product code
Code LFX
Device class
Class 2
Regulation
21 CFR 866.3510
Advisory panel
Microbiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Miami, FL, US
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