Synermed Calcium Reagent Kit

FDA 510(k) K953395 · Synermed, Inc.

Substantially Equivalent

510(k) numberK953395

Submission

Device name
Synermed Calcium Reagent Kit
Applicant
Synermed, Inc.
Quebec, Canada, CA
Received
July 18, 1995
Decision date
August 31, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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.

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K971491Synermed Ir 200 Chemistry AnalyzerJJF · Traditional 06/26/1997SE
K962479Synermed Ise ReagentsCGZ · Traditional 03/03/1997SE
K963939Synermed Direct Bilirubin Reagent KitCIG · Traditional 12/18/1996SE
K960793Synermed Enzymatic CO2 Reagent KitKHS · Traditional 03/11/1996SE
K952179Synermed Ise ReagentsJGS · Traditional 06/20/1995SE
K943924Creatinine-Po Reagent KitCGX · Traditional 09/20/1994SE
K941091Synermed Amylase Reagent KitJFJ · Traditional 05/03/1994SE
K941400Synermed Ise ReagentsJGS · Traditional 04/26/1994SE

Questions and answers

When was Synermed Calcium Reagent Kit cleared by the FDA?

Synermed Calcium Reagent Kit (K953395) received a 510(k) decision of Substantially Equivalent on August 31, 1995, 44 days after the submission was received.

What is the product code of K953395?

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