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FDA 510(k)

SILVERSEAL

K-Number: K040019 · 2004-07-23

Decision Date2004-07-23
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

SILVERSEAL is the device name listed in this FDA 510(k) record. The listed applicant is Noble Fiber Technologies. It received FDA 510(k) clearance on 2004-07-23 under 510(k) number K040019. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILVERSEAL?

SILVERSEAL is a medical device that received FDA 510(k) clearance on 2004-07-23. The listed applicant is Noble Fiber Technologies. The 510(k) number is K040019.

When did SILVERSEAL receive FDA 510(k) clearance?

SILVERSEAL received FDA 510(k) clearance on 2004-07-23, under 510(k) number K040019.

Who is the listed applicant for SILVERSEAL?

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

What is the FDA product code for SILVERSEAL?

The FDA product code for SILVERSEAL is MGQ.

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 Noble Fiber Technologies 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: MGQ)

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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