ALKO FLUIDS PACKS FOR NOVA 8 ANALYZERS
K-Number: K942549 · 1994-07-28
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Device Summary
Frequently Asked Questions
What is the ALKO FLUIDS PACKS FOR NOVA 8 ANALYZERS?
ALKO FLUIDS PACKS FOR NOVA 8 ANALYZERS is a medical device that received FDA 510(k) clearance on 1994-07-28. The listed applicant is Alko Diagnostic Corp.. The 510(k) number is K942549.
When did ALKO FLUIDS PACKS FOR NOVA 8 ANALYZERS receive FDA 510(k) clearance?
ALKO FLUIDS PACKS FOR NOVA 8 ANALYZERS received FDA 510(k) clearance on 1994-07-28, under 510(k) number K942549.
Who is the listed applicant for ALKO FLUIDS PACKS FOR NOVA 8 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 FLUIDS PACKS FOR NOVA 8 ANALYZERS?
The FDA product code for ALKO FLUIDS PACKS FOR NOVA 8 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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