LKB-WALLACE 1250 LUMINOMETER— 510(k) K803131

Name: FDA 510(k) clearance K803131
Creator: U.S. Food and Drug Administration
Published: 1981-01-15

Substantially Equivalent

Lkb Instruments, Inc.

FDA 510(k) clearance K803131 for LKB-WALLACE 1250 LUMINOMETER, Substantially Equivalent on 1981-01-15. Applicant: Lkb Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Lkb Instruments, Inc.
Product code: Code JJQ
Device class: Class 1
Regulation: 21 CFR 862.2300
Advisory panel: Clinical Chemistry
Date received: 1980-12-12
Decision date: 1981-01-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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