SEALGUARD EVAC ENDOTRACHEAL AND ENDOTRACHEAL TUBES
K-Number: K082520 · 2008-10-02
Advertisement
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement