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FDA 510(k)

NOVA 5

K-Number: K811289 · 1981-05-27

Decision Date1981-05-27
Product CodeJGS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NOVA 5 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 1981-05-27 under 510(k) number K811289. 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 5?

NOVA 5 is a medical device that received FDA 510(k) clearance on 1981-05-27. The listed applicant is Nova Biomedical Corp.. The 510(k) number is K811289.

When did NOVA 5 receive FDA 510(k) clearance?

NOVA 5 received FDA 510(k) clearance on 1981-05-27, under 510(k) number K811289.

Who is the listed applicant for NOVA 5?

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 5?

The FDA product code for NOVA 5 is JGS.

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

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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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