ADVIA IMS— 510(k) K001344

Substantially Equivalent

Bayer Corp.

FDA 510(k) clearance K001344 for ADVIA IMS, Substantially Equivalent on 2000-06-26. Applicant: Bayer Corp.. Device class: 1.

Clearance details

Applicant: Bayer Corp.
Product code: Code DIH
Device class: Class 1
Regulation: 21 CFR 862.3240
Advisory panel: Clinical Toxicology
Date received: 2000-04-27
Decision date: 2000-06-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tarrytown, NY, US

Download summary PDF View on FDA.gov ↗

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