Photometric Method, Iron (Non-Heme) (75JIY)

FDA 510(k) K890034 · American Monitor Corp.

Substantially Equivalent

510(k) numberK890034

Submission

Device name
Photometric Method, Iron (Non-Heme) (75JIY)
Applicant
American Monitor Corp.
Indianapolis, IN, US
Received
January 4, 1989
Decision date
February 3, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JIY – Photometric Method, Iron (Non-Heme)
Device class
Class I (low risk)
Regulation
21 CFR 862.1410
Specialty
Clinical Chemistry

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Questions and answers

When was Photometric Method, Iron (Non-Heme) (75JIY) cleared by the FDA?

Photometric Method, Iron (Non-Heme) (75JIY) (K890034) received a 510(k) decision of Substantially Equivalent on February 3, 1989, 30 days after the submission was received.

What is the product code of K890034?

The FDA product code is JIY – Photometric Method, Iron (Non-Heme), a Class I (low risk) device regulated under 21 CFR 862.1410.