CARY 210 SERIES, SPECTROPHOTOMETER— 510(k) K791102

Name: FDA 510(k) clearance K791102
Creator: U.S. Food and Drug Administration
Published: 1979-07-17

Substantially Equivalent

Varian Assoc., Inc.

FDA 510(k) clearance K791102 for CARY 210 SERIES, SPECTROPHOTOMETER, Substantially Equivalent on 1979-07-17. Applicant: Varian Assoc., Inc.. Device class: 1.

Clearance details

Applicant: Varian Assoc., Inc.
Product code: Code JJQ
Device class: Class 1
Regulation: 21 CFR 862.2300
Advisory panel: Clinical Chemistry
Date received: 1979-06-13
Decision date: 1979-07-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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