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FDA 510(k)

NOVA 8 CRT ANALYZER

K-Number: K924547 · 1993-01-28

Decision Date1993-01-28
Product CodeJGS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NOVA 8 CRT 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 1993-01-28 under 510(k) number K924547. 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 NOVA 8 CRT ANALYZER?

NOVA 8 CRT ANALYZER is a medical device that received FDA 510(k) clearance on 1993-01-28. The listed applicant is Nova Biomedical Corp.. The 510(k) number is K924547.

When did NOVA 8 CRT ANALYZER receive FDA 510(k) clearance?

NOVA 8 CRT ANALYZER received FDA 510(k) clearance on 1993-01-28, under 510(k) number K924547.

Who is the listed applicant for NOVA 8 CRT 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 NOVA 8 CRT ANALYZER?

The FDA product code for NOVA 8 CRT 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.

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