SCINTILLATION, LIQUID, RACKBETA— 510(k) K780341

Name: FDA 510(k) clearance K780341
Creator: U.S. Food and Drug Administration
Published: 1978-05-26

Substantially Equivalent

Lkb Instruments, Inc.

FDA 510(k) clearance K780341 for SCINTILLATION, LIQUID, RACKBETA, Substantially Equivalent on 1978-05-26. 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: 1978-03-01
Decision date: 1978-05-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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