Calcium, Scal, Nortrol, Abtrol

FDA 510(k) K073355 · Thermofisher Scientific OY

Substantially Equivalent

510(k) numberK073355

Submission

Device name
Calcium, Scal, Nortrol, Abtrol
Applicant
Thermofisher Scientific OY
Vantaa, FI
Received
November 29, 2007
Decision date
February 28, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CJY – Azo Dye, Calcium
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1145
Specialty
Clinical Chemistry

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More from Ortho-Clinical Diagnostics, Inc.

510(k)DeviceDecision
K110035IndikoJJE · Traditional 06/28/2011SE
K073295Urea/Bun, Scal, Nortrol, AbtrolCDQ · Traditional 05/29/2008SE
K073612Uric Acid (Aox), Scal, Nortrol, AbtrolJIX · Traditional 05/23/2008SE
K073191Alkaline Phosphatase (Ifcc) Plus, Ecal, Nortrol, AbtrolCJE · Traditional 02/28/2008SE
K070824Creatinine (Enzymatic)JFY · Traditional 12/03/2007SE
K071340Carbon Dioxide (CO2), Scal, Nortrol and AbtrolKHS · Traditional 10/05/2007SE
K071580Ast/Got (Ifcc), Pyridoxal Phosphate, Ecal, Nortrol and AbtrolCIT · Traditional 10/03/2007SE

Questions and answers

When was Calcium, Scal, Nortrol, Abtrol cleared by the FDA?

Calcium, Scal, Nortrol, Abtrol (K073355) received a 510(k) decision of Substantially Equivalent on February 28, 2008, 91 days after the submission was received.

What is the product code of K073355?

The FDA product code is CJY – Azo Dye, Calcium, a Class II (moderate risk) device regulated under 21 CFR 862.1145.