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FDA 510(k)

SEALGUARD EVAC ENDOTRACHEAL AND ENDOTRACHEAL TUBES

K-Number: K082520 · 2008-10-02

Decision Date2008-10-02
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SEALGUARD EVAC ENDOTRACHEAL AND ENDOTRACHEAL TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Mallinckrodt Medical. It received FDA 510(k) clearance on 2008-10-02 under 510(k) number K082520. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEALGUARD EVAC ENDOTRACHEAL AND ENDOTRACHEAL TUBES?

SEALGUARD EVAC ENDOTRACHEAL AND ENDOTRACHEAL TUBES is a medical device that received FDA 510(k) clearance on 2008-10-02. The listed applicant is Mallinckrodt Medical. The 510(k) number is K082520.

When did SEALGUARD EVAC ENDOTRACHEAL AND ENDOTRACHEAL TUBES receive FDA 510(k) clearance?

SEALGUARD EVAC ENDOTRACHEAL AND ENDOTRACHEAL TUBES received FDA 510(k) clearance on 2008-10-02, under 510(k) number K082520.

Who is the listed applicant for SEALGUARD EVAC ENDOTRACHEAL AND ENDOTRACHEAL TUBES?

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

What is the FDA product code for SEALGUARD EVAC ENDOTRACHEAL AND ENDOTRACHEAL TUBES?

The FDA product code for SEALGUARD EVAC ENDOTRACHEAL AND ENDOTRACHEAL TUBES is BTR.

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 Mallinckrodt Medical 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 43 devices →

Related Devices (Code: BTR)

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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