CO2 Reagent

FDA 510(k) K880268 · Sigma Diagnostics, Inc.

Substantially Equivalent

510(k) numberK880268

Submission

Device name
CO2 Reagent
Applicant
Sigma Diagnostics, Inc.
St. Louis, MO, US
Received
January 21, 1988
Decision date
March 15, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KHS – Enzymatic, Carbon-Dioxide
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1160
Specialty
Clinical Chemistry

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Questions and answers

When was CO2 Reagent cleared by the FDA?

CO2 Reagent (K880268) received a 510(k) decision of Substantially Equivalent on March 15, 1988, 54 days after the submission was received.

What is the product code of K880268?

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