Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

STAT PROFILE PHOX PLUS ANALYZER

K-Number: K000895 · 2000-04-17

Decision Date2000-04-17
Product CodeJGS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

STAT PROFILE PHOX PLUS ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Nova Biomedical Corp.. It received FDA 510(k) clearance on 2000-04-17 under 510(k) number K000895. The device is classified under product code JGS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAT PROFILE PHOX PLUS ANALYZER?

STAT PROFILE PHOX PLUS ANALYZER is a medical device that received FDA 510(k) clearance on 2000-04-17. The listed applicant is Nova Biomedical Corp.. The 510(k) number is K000895.

When did STAT PROFILE PHOX PLUS ANALYZER receive FDA 510(k) clearance?

STAT PROFILE PHOX PLUS ANALYZER received FDA 510(k) clearance on 2000-04-17, under 510(k) number K000895.

Who is the listed applicant for 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 STAT PROFILE PHOX PLUS ANALYZER?

The FDA product code for STAT PROFILE PHOX PLUS ANALYZER is JGS.

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.

View all 89 devices →

Related Devices (Code: JGS)

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.

↑