LYTETEK SYSTEM— 510(k) K770774

Substantially Equivalent

Boehringer Mannheim Corp.

FDA 510(k) clearance K770774 for LYTETEK SYSTEM, Substantially Equivalent on 1977-07-11. Applicant: Boehringer Mannheim Corp.. Device class: 2.

Clearance details

Applicant: Boehringer Mannheim Corp.
Product code: Code JGT
Device class: Class 2
Regulation: 21 CFR 862.1665
Advisory panel: Clinical Chemistry
Date received: 1977-04-28
Decision date: 1977-07-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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