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FDA 510(k)

STAT PROFILE ULTRA 11 ANALYZER

K-Number: K943643 · 1994-12-29

Decision Date1994-12-29
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

STAT PROFILE ULTRA 11 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 1994-12-29 under 510(k) number K943643. The device is classified under product code CHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAT PROFILE ULTRA 11 ANALYZER?

STAT PROFILE ULTRA 11 ANALYZER is a medical device that received FDA 510(k) clearance on 1994-12-29. The listed applicant is Nova Biomedical Corp.. The 510(k) number is K943643.

When did STAT PROFILE ULTRA 11 ANALYZER receive FDA 510(k) clearance?

STAT PROFILE ULTRA 11 ANALYZER received FDA 510(k) clearance on 1994-12-29, under 510(k) number K943643.

Who is the listed applicant for STAT PROFILE ULTRA 11 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 ULTRA 11 ANALYZER?

The FDA product code for STAT PROFILE ULTRA 11 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.

View all 89 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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