Sigma Diagnostics CO2 Acid Reagent

FDA 510(k) K963541 · Sigma Diagnostics, Inc.

Substantially Equivalent

510(k) numberK963541

Submission

Device name
Sigma Diagnostics CO2 Acid Reagent
Applicant
Sigma Diagnostics, Inc.
St. Louis, MO, US
Received
September 4, 1996
Decision date
October 24, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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

Other 510(k)s with product code JFL

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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
K933695Sigma Electrolyte BufferJFL · Traditional Sigma Chemical Co.10/22/1993SE

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Questions and answers

When was Sigma Diagnostics CO2 Acid Reagent cleared by the FDA?

Sigma Diagnostics CO2 Acid Reagent (K963541) received a 510(k) decision of Substantially Equivalent on October 24, 1996, 50 days after the submission was received.

What is the product code of K963541?

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