1205 BETAPLATE LIQUID SCINTILLATION COUNTER— 510(k) K874094

Name: FDA 510(k) clearance K874094
Creator: U.S. Food and Drug Administration
Published: 1987-11-04

Substantially Equivalent

Lkb Instruments, Inc.

FDA 510(k) clearance K874094 for 1205 BETAPLATE LIQUID SCINTILLATION COUNTER, Substantially Equivalent on 1987-11-04. Applicant: Lkb Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Lkb Instruments, Inc.
Product code: Code JJJ
Device class: Class 1
Regulation: 21 CFR 862.2320
Advisory panel: Clinical Chemistry
Date received: 1987-09-30
Decision date: 1987-11-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gaithersburg, MD, US

Download summary PDF View on FDA.gov ↗

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