OSMOMETER MODEL 2400— 510(k) K911092

Name: FDA 510(k) clearance K911092
Creator: U.S. Food and Drug Administration
Published: 1991-05-22

Substantially Equivalent

Advanced Instruments, Inc.

FDA 510(k) clearance K911092 for OSMOMETER MODEL 2400, Substantially Equivalent on 1991-05-22. Applicant: Advanced Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Advanced Instruments, Inc.
Product code: Code JJM
Device class: Class 1
Regulation: 21 CFR 862.2730
Advisory panel: Clinical Chemistry
Date received: 1991-03-11
Decision date: 1991-05-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Needham Heights, MA, US

Download summary PDF View on FDA.gov ↗

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