Olympus Calcium Reagent

FDA 510(k) K924435 · Olympus Corp.

Substantially Equivalent

510(k) numberK924435

Submission

Device name
Olympus Calcium Reagent
Applicant
Olympus Corp.
Lake Success, NY, US
Received
September 1, 1992
Decision date
October 19, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
CIC – Cresolphthalein Complexone, Calcium
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1145
Specialty
Clinical Chemistry

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Questions and answers

When was Olympus Calcium Reagent cleared by the FDA?

Olympus Calcium Reagent (K924435) received a 510(k) decision of Substantially Equivalent on October 19, 1992, 48 days after the submission was received.

What is the product code of K924435?

The FDA product code is CIC – Cresolphthalein Complexone, Calcium, a Class II (moderate risk) device regulated under 21 CFR 862.1145.