ALKO CAL PACKS FOR CORNING 654 ANALYZERS
K-Number: K944922 · 1995-02-10
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Device Summary
Frequently Asked Questions
What is the ALKO CAL PACKS FOR CORNING 654 ANALYZERS?
ALKO CAL PACKS FOR CORNING 654 ANALYZERS is a medical device that received FDA 510(k) clearance on 1995-02-10. The listed applicant is Alko Diagnostic Corp.. The 510(k) number is K944922.
When did ALKO CAL PACKS FOR CORNING 654 ANALYZERS receive FDA 510(k) clearance?
ALKO CAL PACKS FOR CORNING 654 ANALYZERS received FDA 510(k) clearance on 1995-02-10, under 510(k) number K944922.
Who is the listed applicant for ALKO CAL PACKS FOR CORNING 654 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 ALKO CAL PACKS FOR CORNING 654 ANALYZERS?
The FDA product code for ALKO CAL PACKS FOR CORNING 654 ANALYZERS 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 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.
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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