Nova 11 Na/K/Li Analyzer

FDA 510(k) K915178 · Nova Biomedical Corp.

Substantially Equivalent

510(k) numberK915178

Submission

Device name
Nova 11 Na/K/Li Analyzer
Applicant
Nova Biomedical Corp.
Walham, MA, US
Received
November 15, 1991
Decision date
January 27, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
CEM – Electrode, Ion Specific, Potassium
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1600
Specialty
Clinical Chemistry

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Questions and answers

When was Nova 11 Na/K/Li Analyzer cleared by the FDA?

Nova 11 Na/K/Li Analyzer (K915178) received a 510(k) decision of Substantially Equivalent on January 27, 1992, 73 days after the submission was received.

What is the product code of K915178?

The FDA product code is CEM – Electrode, Ion Specific, Potassium, a Class II (moderate risk) device regulated under 21 CFR 862.1600.