ULTROSPEC W/APPLE II -4050-— 510(k) K834489

Name: FDA 510(k) clearance K834489
Creator: U.S. Food and Drug Administration
Published: 1984-02-10

Substantially Equivalent

Lkb Instruments, Inc.

FDA 510(k) clearance K834489 for ULTROSPEC W/APPLE II -4050-, Substantially Equivalent on 1984-02-10. 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: 1983-12-02
Decision date: 1984-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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