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FDA 510(k)

NOVA 13 ANALYZER, MODIFICATION

K-Number: K924864 · 1992-11-06

ApplicantNova Biomedical Corp.
Decision Date1992-11-06
Product CodeCGZ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NOVA 13 ANALYZER, MODIFICATION 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 1992-11-06 under 510(k) number K924864. The device is classified under product code CGZ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVA 13 ANALYZER, MODIFICATION?

NOVA 13 ANALYZER, MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-11-06. The listed applicant is Nova Biomedical Corp.. The 510(k) number is K924864.

When did NOVA 13 ANALYZER, MODIFICATION receive FDA 510(k) clearance?

NOVA 13 ANALYZER, MODIFICATION received FDA 510(k) clearance on 1992-11-06, under 510(k) number K924864.

Who is the listed applicant for NOVA 13 ANALYZER, MODIFICATION?

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 13 ANALYZER, MODIFICATION?

The FDA product code for NOVA 13 ANALYZER, MODIFICATION is CGZ.

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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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