PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE
K-Number: K133043 · 2013-12-06
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Device Summary
Frequently Asked Questions
What is the PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE?
PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE is a medical device that received FDA 510(k) clearance on 2013-12-06. The listed applicant is Angioslide, Ltd.. The 510(k) number is K133043.
When did PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE receive FDA 510(k) clearance?
PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE received FDA 510(k) clearance on 2013-12-06, under 510(k) number K133043.
Who is the listed applicant for PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE?
The FDA 510(k) record lists Angioslide, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE?
The FDA product code for PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE 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 Angioslide, Ltd. 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.
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