CALIBRATING MATERIAL, ISE ELECTROLYTE REFERENCE
K-Number: K033061 · 2003-11-07
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Device Summary
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.
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
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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