MULTI ANALYTE MIXTURE, CALIBRATORS
K-Number: K902675 · 1990-07-31
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Device Summary
Frequently Asked Questions
What is the MULTI ANALYTE MIXTURE, CALIBRATORS?
MULTI ANALYTE MIXTURE, CALIBRATORS is a medical device that received FDA 510(k) clearance on 1990-07-31. The listed applicant is Phoenix Diagnostics, Inc.. The 510(k) number is K902675.
When did MULTI ANALYTE MIXTURE, CALIBRATORS receive FDA 510(k) clearance?
MULTI ANALYTE MIXTURE, CALIBRATORS received FDA 510(k) clearance on 1990-07-31, under 510(k) number K902675.
Who is the listed applicant for MULTI ANALYTE MIXTURE, CALIBRATORS?
The FDA 510(k) record lists Phoenix Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTI ANALYTE MIXTURE, CALIBRATORS?
The FDA product code for MULTI ANALYTE MIXTURE, CALIBRATORS 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 Phoenix 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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