Paramax Total Iron Binding Capacity Pretreatment

FDA 510(k) K923569 · Baxter Diagnostics, Inc.

Substantially Equivalent

510(k) numberK923569

Submission

Device name
Paramax Total Iron Binding Capacity Pretreatment
Applicant
Baxter Diagnostics, Inc.
Santa Ana, CA, US
Received
July 17, 1992
Decision date
August 26, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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 Paramax Total Iron Binding Capacity Pretreatment cleared by the FDA?

Paramax Total Iron Binding Capacity Pretreatment (K923569) received a 510(k) decision of Substantially Equivalent on August 26, 1992, 40 days after the submission was received.

What is the product code of K923569?

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