CATHETERS FOR BALLOON OCCLUSION FEMORAL ANGIOGRAPH
K-Number: K892530 · 1989-09-26
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Device Summary
Frequently Asked Questions
What is the CATHETERS FOR BALLOON OCCLUSION FEMORAL ANGIOGRAPH?
CATHETERS FOR BALLOON OCCLUSION FEMORAL ANGIOGRAPH is a medical device that received FDA 510(k) clearance on 1989-09-26. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K892530.
When did CATHETERS FOR BALLOON OCCLUSION FEMORAL ANGIOGRAPH receive FDA 510(k) clearance?
CATHETERS FOR BALLOON OCCLUSION FEMORAL ANGIOGRAPH received FDA 510(k) clearance on 1989-09-26, under 510(k) number K892530.
Who is the listed applicant for CATHETERS FOR BALLOON OCCLUSION FEMORAL ANGIOGRAPH?
The FDA 510(k) record lists Arrow Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CATHETERS FOR BALLOON OCCLUSION FEMORAL ANGIOGRAPH?
The FDA product code for CATHETERS FOR BALLOON OCCLUSION FEMORAL ANGIOGRAPH is DYG.
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 Arrow Intl., 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: DYG)
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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