USCI HEMAQUET XT INTRODUCER
K-Number: K920251 · 1992-03-18
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Device Summary
Frequently Asked Questions
What is the USCI HEMAQUET XT INTRODUCER?
USCI HEMAQUET XT INTRODUCER is a medical device that received FDA 510(k) clearance on 1992-03-18. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K920251.
When did USCI HEMAQUET XT INTRODUCER receive FDA 510(k) clearance?
USCI HEMAQUET XT INTRODUCER received FDA 510(k) clearance on 1992-03-18, under 510(k) number K920251.
Who is the listed applicant for USCI HEMAQUET XT INTRODUCER?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for USCI HEMAQUET XT INTRODUCER?
The FDA product code for USCI HEMAQUET XT INTRODUCER is DYB.
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 C.R. Bard, Inc. 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: DYB)
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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