OPTIV ANTAGE DH POWER INJECTION SYSTEM
K-Number: K042744 · 2004-11-30
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Device Summary
Frequently Asked Questions
What is the OPTIV ANTAGE DH POWER INJECTION SYSTEM?
OPTIV ANTAGE DH POWER INJECTION SYSTEM is a medical device that received FDA 510(k) clearance on 2004-11-30. The listed applicant is Mallinckrodt Inc., Liebel-Flarsheim Business. The 510(k) number is K042744.
When did OPTIV ANTAGE DH POWER INJECTION SYSTEM receive FDA 510(k) clearance?
OPTIV ANTAGE DH POWER INJECTION SYSTEM received FDA 510(k) clearance on 2004-11-30, under 510(k) number K042744.
Who is the listed applicant for OPTIV ANTAGE DH POWER INJECTION SYSTEM?
The FDA 510(k) record lists Mallinckrodt Inc., Liebel-Flarsheim Business as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OPTIV ANTAGE DH POWER INJECTION SYSTEM?
The FDA product code for OPTIV ANTAGE DH POWER INJECTION SYSTEM is DXT.
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 Inc., Liebel-Flarsheim Business 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: DXT)
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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