Ise/Ci-

FDA 510(k) K912647 · Boehringer Mannheim Corp.

Substantially Equivalent

510(k) numberK912647

Submission

Device name
Ise/Ci-
Applicant
Boehringer Mannheim Corp.
Indianapolis, IN, US
Received
June 17, 1991
Decision date
July 17, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CGZ – Electrode, Ion-Specific, Chloride
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1170
Specialty
Clinical Chemistry

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More from Phoenix Diagnostics, Inc.

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K984425Modification of Preciset Serum Proteins CalibratorJIX · Traditional 01/20/1999SE
K984372Elecsys Calcheck Troponin TJJY · Traditional 12/14/1998SE
K984105Elecsys Troponin T Stat TestMMI · Traditional 12/08/1998SE
K983503Roche Diagnostics, Boehringer Mannheim Corporation Inorganic Phosphorus Reagent Catalog…CEO · Traditional 12/01/1998SE
K983469Preciset Serum Proteins CalibratorJIX · Traditional 11/25/1998SE
K983185Boehringer Mannheim Tina-Quant Ige TestDGC · Traditional 11/12/1998SE
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Questions and answers

When was Ise/Ci- cleared by the FDA?

Ise/Ci- (K912647) received a 510(k) decision of Substantially Equivalent on July 17, 1991, 30 days after the submission was received.

What is the product code of K912647?

The FDA product code is CGZ – Electrode, Ion-Specific, Chloride, a Class II (moderate risk) device regulated under 21 CFR 862.1170.