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FDA 510(k)

SODIUM AND POTASSIUM STANDARD

K-Number: K895717 · 1990-01-11

ApplicantData Medical Associates, Inc.
Decision Date1990-01-11
Product CodeJIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SODIUM AND POTASSIUM STANDARD is the device name listed in this FDA 510(k) record. The listed applicant is Data Medical Associates, Inc.. It received FDA 510(k) clearance on 1990-01-11 under 510(k) number K895717. The device is classified under product code JIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SODIUM AND POTASSIUM STANDARD?

SODIUM AND POTASSIUM STANDARD is a medical device that received FDA 510(k) clearance on 1990-01-11. The listed applicant is Data Medical Associates, Inc.. The 510(k) number is K895717.

When did SODIUM AND POTASSIUM STANDARD receive FDA 510(k) clearance?

SODIUM AND POTASSIUM STANDARD received FDA 510(k) clearance on 1990-01-11, under 510(k) number K895717.

Who is the listed applicant for SODIUM AND POTASSIUM STANDARD?

The FDA 510(k) record lists Data Medical Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SODIUM AND POTASSIUM STANDARD?

The FDA product code for SODIUM AND POTASSIUM STANDARD is JIX.

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Other records listing Data Medical Associates, Inc. as applicant

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Related Devices (Code: JIX)

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K161140VITROS Chemistry Products Calibrator Kit 3Ortho-Clinical Diagnostics, Inc.K133330C.F.A.S. PROTEINS, C.F.A.S. PAC, PRECICONTROL CLINCHEM MULTI 1 & 2, PRECINORM PROTEIN & PRECIPATH PROTEINRoche DiagnosticsK130765ELITECH CLINICAL SYSTEMS ELICAL 2; ELITECH CLINICAL SYSTEMS ELITROL I, ELITECH CLINICAL SYSTEMS ELITROL IIElitechgroupK123321DIMENSION CHEMISTRY III CALIBRATORYSiemens Healthcare DiagnosticsK123372ABBOTT LIPID MULTI CONSTITUENT CALIBRATORAbbott LaboratoriesK122398RAPIDPOINT 500 SYSTEM MEASUREMENT CARTRIDGE WITH CALIBRATORSSiemens Healthcare Diagnostics, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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