SECURELOC; ADVANCINTRODUCER
K-Number: K050023 · 2005-02-18
Advertisement
Device Summary
Frequently Asked Questions
What is the SECURELOC; ADVANCINTRODUCER?
SECURELOC; ADVANCINTRODUCER is a medical device that received FDA 510(k) clearance on 2005-02-18. The listed applicant is Specialized Health Products, Inc.. The 510(k) number is K050023.
When did SECURELOC; ADVANCINTRODUCER receive FDA 510(k) clearance?
SECURELOC; ADVANCINTRODUCER received FDA 510(k) clearance on 2005-02-18, under 510(k) number K050023.
Who is the listed applicant for SECURELOC; ADVANCINTRODUCER?
The FDA 510(k) record lists Specialized Health Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SECURELOC; ADVANCINTRODUCER?
The FDA product code for SECURELOC; ADVANCINTRODUCER 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 Specialized Health 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