BRAIDED GUIDING INTRODUCER
K-Number: K004026 · 2001-07-09
Advertisement
Device Summary
Frequently Asked Questions
What is the BRAIDED GUIDING INTRODUCER?
BRAIDED GUIDING INTRODUCER is a medical device that received FDA 510(k) clearance on 2001-07-09. The listed applicant is Thomas Medical Products, Inc.. The 510(k) number is K004026.
When did BRAIDED GUIDING INTRODUCER receive FDA 510(k) clearance?
BRAIDED GUIDING INTRODUCER received FDA 510(k) clearance on 2001-07-09, under 510(k) number K004026.
Who is the listed applicant for BRAIDED GUIDING INTRODUCER?
The FDA 510(k) record lists Thomas Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BRAIDED GUIDING INTRODUCER?
The FDA product code for BRAIDED 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 Thomas Medical Products, 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.
Advertisement