SWARTZ BRAIDED TRANSSEPTAL GUIDING INTRODUCER
K-Number: K052644 · 2005-12-05
Advertisement
Device Summary
Frequently Asked Questions
What is the SWARTZ BRAIDED TRANSSEPTAL GUIDING INTRODUCER?
SWARTZ BRAIDED TRANSSEPTAL GUIDING INTRODUCER is a medical device that received FDA 510(k) clearance on 2005-12-05. The listed applicant is St Jude Medical. The 510(k) number is K052644.
When did SWARTZ BRAIDED TRANSSEPTAL GUIDING INTRODUCER receive FDA 510(k) clearance?
SWARTZ BRAIDED TRANSSEPTAL GUIDING INTRODUCER received FDA 510(k) clearance on 2005-12-05, under 510(k) number K052644.
Who is the listed applicant for SWARTZ BRAIDED TRANSSEPTAL GUIDING INTRODUCER?
The FDA 510(k) record lists St Jude Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SWARTZ BRAIDED TRANSSEPTAL GUIDING INTRODUCER?
The FDA product code for SWARTZ BRAIDED TRANSSEPTAL GUIDING 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 St Jude 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: 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.
Advertisement