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FDA 510(k)

COVERUPS

K-Number: K831703 · 1984-01-03

Decision Date1984-01-03
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COVERUPS is the device name listed in this FDA 510(k) record. The listed applicant is The Urology Group. It received FDA 510(k) clearance on 1984-01-03 under 510(k) number K831703. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COVERUPS?

COVERUPS is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is The Urology Group. The 510(k) number is K831703.

When did COVERUPS receive FDA 510(k) clearance?

COVERUPS received FDA 510(k) clearance on 1984-01-03, under 510(k) number K831703.

Who is the listed applicant for COVERUPS?

The FDA 510(k) record lists The Urology Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COVERUPS?

The FDA product code for COVERUPS is NAD.

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 The Urology Group 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.

Related Devices (Code: NAD)

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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