Ca Buffer Ca Dye

FDA 510(k) K852002 · Alpkem Corp.

Substantially Equivalent

510(k) numberK852002

Submission

Device name
Ca Buffer Ca Dye
Applicant
Alpkem Corp.
Clackamas, OR, US
Received
May 7, 1985
Decision date
June 25, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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K890333Albumin ReagentEIX · Traditional 02/17/1989SE
K890332RFA/2 Rapid Flow Analyzer W/ComputerJJC · Traditional 02/17/1989SE
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Questions and answers

When was Ca Buffer Ca Dye cleared by the FDA?

Ca Buffer Ca Dye (K852002) received a 510(k) decision of Substantially Equivalent on June 25, 1985, 49 days after the submission was received.

What is the product code of K852002?

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