SOLOPATH BALLOON EXPANDABLE TRANSFEMORAL INTRODUCER
K-Number: K092014 · 2009-10-08
Advertisement
Device Summary
Frequently Asked Questions
What is the SOLOPATH BALLOON EXPANDABLE TRANSFEMORAL INTRODUCER?
SOLOPATH BALLOON EXPANDABLE TRANSFEMORAL INTRODUCER is a medical device that received FDA 510(k) clearance on 2009-10-08. The listed applicant is Onset Medical Corporation. The 510(k) number is K092014.
When did SOLOPATH BALLOON EXPANDABLE TRANSFEMORAL INTRODUCER receive FDA 510(k) clearance?
SOLOPATH BALLOON EXPANDABLE TRANSFEMORAL INTRODUCER received FDA 510(k) clearance on 2009-10-08, under 510(k) number K092014.
Who is the listed applicant for SOLOPATH BALLOON EXPANDABLE TRANSFEMORAL INTRODUCER?
The FDA 510(k) record lists Onset Medical Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SOLOPATH BALLOON EXPANDABLE TRANSFEMORAL INTRODUCER?
The FDA product code for SOLOPATH BALLOON EXPANDABLE TRANSFEMORAL 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 Onset Medical Corporation 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