Nova 3+3 Chloride/Total Carbon Dioxide

FDA 510(k) K792254 · Nova Biomedical Corp.

Substantially Equivalent

510(k) numberK792254

Submission

Device name
Nova 3+3 Chloride/Total Carbon Dioxide
Applicant
Nova Biomedical Corp.
Mchenry, IL, US
Received
November 8, 1979
Decision date
December 6, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JFL – Ph Rate Measurement, Carbon-Dioxide
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1160
Specialty
Clinical Chemistry

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K963541Sigma Diagnostics CO2 Acid ReagentJFL · Traditional Sigma Diagnostics, Inc.10/24/1996SE
K963538Sigma Diagnostics CO2ALKALINE BufferJFL · Traditional Sigma Diagnostics, Inc.10/11/1996SE
K963540Sigma Diagnostics Electrolyte BufferJFL · Traditional Sigma Diagnostics, Inc.09/27/1996SE
K963005Nova 16 Analyzer (Modification Point of Care Usage)JFL · Traditional Nova Biomedical Corp.08/23/1996SE
K933696Sigma Electrolyte Reference ReagentJFL · Traditional Sigma Chemical Co.01/03/1994SE
K933691Sigma CO2 Alkaline Buffer ReagentJFL · Traditional Sigma Chemical Co.12/17/1993SE
K933692Sigma CO2 Acid ReagentJFL · Traditional Sigma Chemical Co.12/09/1993SE

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Questions and answers

When was Nova 3+3 Chloride/Total Carbon Dioxide cleared by the FDA?

Nova 3+3 Chloride/Total Carbon Dioxide (K792254) received a 510(k) decision of Substantially Equivalent on December 6, 1979, 28 days after the submission was received.

What is the product code of K792254?

The FDA product code is JFL – Ph Rate Measurement, Carbon-Dioxide, a Class II (moderate risk) device regulated under 21 CFR 862.1160.