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FDA 510(k)

CALIBRATING MATERIAL, ISE ELECTROLYTE REFERENCE

K-Number: K033061 · 2003-11-07

Decision Date2003-11-07
Product CodeJIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CALIBRATING MATERIAL, ISE ELECTROLYTE REFERENCE is the device name listed in this FDA 510(k) record. The listed applicant is Diamond Diagnostics, Inc.. It received FDA 510(k) clearance on 2003-11-07 under 510(k) number K033061. 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 CALIBRATING MATERIAL, ISE ELECTROLYTE REFERENCE?

CALIBRATING MATERIAL, ISE ELECTROLYTE REFERENCE is a medical device that received FDA 510(k) clearance on 2003-11-07. The listed applicant is Diamond Diagnostics, Inc.. The 510(k) number is K033061.

When did CALIBRATING MATERIAL, ISE ELECTROLYTE REFERENCE receive FDA 510(k) clearance?

CALIBRATING MATERIAL, ISE ELECTROLYTE REFERENCE received FDA 510(k) clearance on 2003-11-07, under 510(k) number K033061.

Who is the listed applicant for CALIBRATING MATERIAL, ISE ELECTROLYTE REFERENCE?

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

What is the FDA product code for CALIBRATING MATERIAL, ISE ELECTROLYTE REFERENCE?

The FDA product code for CALIBRATING MATERIAL, ISE ELECTROLYTE REFERENCE is JIX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Diamond Diagnostics, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: JIX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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

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