ISE CALIBRATORS FOR CORNING 600 SERIES ANALYZERS
K-Number: K930796 · 1994-01-13
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Device Summary
Frequently Asked Questions
What is the ISE CALIBRATORS FOR CORNING 600 SERIES ANALYZERS?
ISE CALIBRATORS FOR CORNING 600 SERIES ANALYZERS is a medical device that received FDA 510(k) clearance on 1994-01-13. The listed applicant is Alko Diagnostic Corp.. The 510(k) number is K930796.
When did ISE CALIBRATORS FOR CORNING 600 SERIES ANALYZERS receive FDA 510(k) clearance?
ISE CALIBRATORS FOR CORNING 600 SERIES ANALYZERS received FDA 510(k) clearance on 1994-01-13, under 510(k) number K930796.
Who is the listed applicant for ISE CALIBRATORS FOR CORNING 600 SERIES ANALYZERS?
The FDA 510(k) record lists Alko Diagnostic Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ISE CALIBRATORS FOR CORNING 600 SERIES ANALYZERS?
The FDA product code for ISE CALIBRATORS FOR CORNING 600 SERIES ANALYZERS is JZX.
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 Alko Diagnostic Corp. 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.
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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