MODIFICATION TO STAT PROFILE PHOX PLUS ANALYZER
K-Number: K002613 · 2000-10-19
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Device Summary
Frequently Asked Questions
What is the MODIFICATION TO STAT PROFILE PHOX PLUS ANALYZER?
MODIFICATION TO STAT PROFILE PHOX PLUS ANALYZER is a medical device that received FDA 510(k) clearance on 2000-10-19. The listed applicant is Nova Biomedical Corp.. The 510(k) number is K002613.
When did MODIFICATION TO STAT PROFILE PHOX PLUS ANALYZER receive FDA 510(k) clearance?
MODIFICATION TO STAT PROFILE PHOX PLUS ANALYZER received FDA 510(k) clearance on 2000-10-19, under 510(k) number K002613.
Who is the listed applicant for MODIFICATION TO STAT PROFILE PHOX PLUS ANALYZER?
The FDA 510(k) record lists Nova Biomedical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFICATION TO STAT PROFILE PHOX PLUS ANALYZER?
The FDA product code for MODIFICATION TO STAT PROFILE PHOX PLUS ANALYZER is CHL.
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 Nova Biomedical 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: CHL)
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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