Kodak Ektachem Clinical Chemistry Slides (Fe)

FDA 510(k) K884355 · Eastman Kodak Company

Substantially Equivalent

510(k) numberK884355

Submission

Device name
Kodak Ektachem Clinical Chemistry Slides (Fe)
Applicant
Eastman Kodak Company
Rochester, NY, US
Received
October 17, 1988
Decision date
December 16, 1988
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 Kodak Ektachem Clinical Chemistry Slides (Fe) cleared by the FDA?

Kodak Ektachem Clinical Chemistry Slides (Fe) (K884355) received a 510(k) decision of Substantially Equivalent on December 16, 1988, 60 days after the submission was received.

What is the product code of K884355?

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