GLIDER PTA BALLOON CATHETER
K-Number: K101062 · 2010-05-12
Advertisement
Device Summary
Frequently Asked Questions
What is the GLIDER PTA BALLOON CATHETER?
GLIDER PTA BALLOON CATHETER is a medical device that received FDA 510(k) clearance on 2010-05-12. The listed applicant is Trireme Medical, Inc.. The 510(k) number is K101062.
When did GLIDER PTA BALLOON CATHETER receive FDA 510(k) clearance?
GLIDER PTA BALLOON CATHETER received FDA 510(k) clearance on 2010-05-12, under 510(k) number K101062.
Who is the listed applicant for GLIDER PTA BALLOON CATHETER?
The FDA 510(k) record lists Trireme Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GLIDER PTA BALLOON CATHETER?
The FDA product code for GLIDER PTA BALLOON CATHETER is LIT.
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 Trireme Medical, 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: LIT)
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