LASER IMMUNONEPHELOMETRIC ANALYZER— 510(k) K772361

Name: FDA 510(k) clearance K772361
Creator: U.S. Food and Drug Administration
Published: 1978-01-30

Substantially Equivalent

G.D. Searle and Co.

FDA 510(k) clearance K772361 for LASER IMMUNONEPHELOMETRIC ANALYZER, Substantially Equivalent on 1978-01-30. Applicant: G.D. Searle and Co.. Device class: 1.

Clearance details

Applicant: G.D. Searle and Co.
Product code: Code JQX
Device class: Class 1
Regulation: 21 CFR 862.2700
Advisory panel: Clinical Chemistry
Date received: 1977-12-27
Decision date: 1978-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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