BILIRUBIN, DINGLE VALVE DPD— 510(k) K781921

Name: FDA 510(k) clearance K781921
Creator: U.S. Food and Drug Administration
Published: 1979-01-03

Substantially Equivalent

Boehringer Mannheim Corp.

FDA 510(k) clearance K781921 for BILIRUBIN, DINGLE VALVE DPD, Substantially Equivalent on 1979-01-03. Applicant: Boehringer Mannheim Corp.. Device class: 2.

Clearance details

Applicant: Boehringer Mannheim Corp.
Product code: Code CIG
Device class: Class 2
Regulation: 21 CFR 862.1110
Advisory panel: Clinical Chemistry
Date received: 1978-11-13
Decision date: 1979-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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