Iron/Uibc Reagent

FDA 510(k) K932517 · Sigma Diagnostics, Inc.

Substantially Equivalent

510(k) numberK932517

Submission

Device name
Iron/Uibc Reagent
Applicant
Sigma Diagnostics, Inc.
St. Louis, MO, US
Received
May 25, 1993
Decision date
November 9, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JMO – Ferrozine (Colorimetric) Iron Binding Capacity
Device class
Class I (low risk)
Regulation
21 CFR 862.1415
Specialty
Clinical Chemistry

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Questions and answers

When was Iron/Uibc Reagent cleared by the FDA?

Iron/Uibc Reagent (K932517) received a 510(k) decision of Substantially Equivalent on November 9, 1993, 168 days after the submission was received.

What is the product code of K932517?

The FDA product code is JMO – Ferrozine (Colorimetric) Iron Binding Capacity, a Class I (low risk) device regulated under 21 CFR 862.1415.