PREMIER PLATINUM HPSA PLUS, MODELS 601396, 601480
K-Number: K053335 · 2006-03-10
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Device Summary
Frequently Asked Questions
What is the PREMIER PLATINUM HPSA PLUS, MODELS 601396, 601480?
PREMIER PLATINUM HPSA PLUS, MODELS 601396, 601480 is a medical device that received FDA 510(k) clearance on 2006-03-10. The listed applicant is Meridian Bioscience, Inc.. The 510(k) number is K053335.
When did PREMIER PLATINUM HPSA PLUS, MODELS 601396, 601480 receive FDA 510(k) clearance?
PREMIER PLATINUM HPSA PLUS, MODELS 601396, 601480 received FDA 510(k) clearance on 2006-03-10, under 510(k) number K053335.
Who is the listed applicant for PREMIER PLATINUM HPSA PLUS, MODELS 601396, 601480?
The FDA 510(k) record lists Meridian Bioscience, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PREMIER PLATINUM HPSA PLUS, MODELS 601396, 601480?
The FDA product code for PREMIER PLATINUM HPSA PLUS, MODELS 601396, 601480 is LYR.
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 Meridian Bioscience, 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: LYR)
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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