Stratus Estradiol Fluoremetric Enzyme

FDA 510(k) K910249 · Baxter Healthcare Corp

Substantially Equivalent

510(k) numberK910249

Submission

Device name
Stratus Estradiol Fluoremetric Enzyme
Applicant
Baxter Healthcare Corp
Miami, FL, US
Received
January 22, 1991
Decision date
February 13, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CHP – Radioimmunoassay, Estradiol
Device class
Class I (low risk)
Regulation
21 CFR 862.1260
Specialty
Clinical Chemistry

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Questions and answers

When was Stratus Estradiol Fluoremetric Enzyme cleared by the FDA?

Stratus Estradiol Fluoremetric Enzyme (K910249) received a 510(k) decision of Substantially Equivalent on February 13, 1991, 22 days after the submission was received.

What is the product code of K910249?

The FDA product code is CHP – Radioimmunoassay, Estradiol, a Class I (low risk) device regulated under 21 CFR 862.1260.