CALCIUM/MAGNESIUM ANALYZER— 510(k) K770570

Name: FDA 510(k) clearance K770570
Creator: U.S. Food and Drug Administration
Published: 1977-06-08

Substantially Equivalent

Beckman Instruments, Inc.

FDA 510(k) clearance K770570 for CALCIUM/MAGNESIUM ANALYZER, Substantially Equivalent on 1977-06-08. Applicant: Beckman Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Beckman Instruments, Inc.
Product code: Code JFN
Device class: Class 2
Regulation: 21 CFR 862.1145
Advisory panel: Clinical Chemistry
Date received: 1977-03-25
Decision date: 1977-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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