ULTROSPEC K KINETICS SPECTROPHOTOMETER— 510(k) K861194

Name: FDA 510(k) clearance K861194
Creator: U.S. Food and Drug Administration
Published: 1986-04-24

Substantially Equivalent

Lkb Instruments, Inc.

FDA 510(k) clearance K861194 for ULTROSPEC K KINETICS SPECTROPHOTOMETER, Substantially Equivalent on 1986-04-24. 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: 1986-03-31
Decision date: 1986-04-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gaithersburg, MD, US

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