Stratus(R) Gentamicin Fluorometric Enzyme Immuno.

FDA 510(k) K895484 · Baxter Healthcare Corp

Substantially Equivalent

510(k) numberK895484

Submission

Device name
Stratus(R) Gentamicin Fluorometric Enzyme Immuno.
Applicant
Baxter Healthcare Corp
Miami, FL, US
Received
September 11, 1989
Decision date
October 4, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LCD – Enzyme Immunoassay, Gentamicin
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3450
Specialty
Clinical Toxicology

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Questions and answers

When was Stratus(R) Gentamicin Fluorometric Enzyme Immuno. cleared by the FDA?

Stratus(R) Gentamicin Fluorometric Enzyme Immuno. (K895484) received a 510(k) decision of Substantially Equivalent on October 4, 1989, 23 days after the submission was received.

What is the product code of K895484?

The FDA product code is LCD – Enzyme Immunoassay, Gentamicin, a Class II (moderate risk) device regulated under 21 CFR 862.3450.