METRONIC BUCHBINDER ENVOY PERCUTANEOUS CATHETERS
K-Number: K935425 · 1994-04-26
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Device Summary
Frequently Asked Questions
What is the METRONIC BUCHBINDER ENVOY PERCUTANEOUS CATHETERS?
METRONIC BUCHBINDER ENVOY PERCUTANEOUS CATHETERS is a medical device that received FDA 510(k) clearance on 1994-04-26. The listed applicant is Medtronics Interventional Vascular. The 510(k) number is K935425.
When did METRONIC BUCHBINDER ENVOY PERCUTANEOUS CATHETERS receive FDA 510(k) clearance?
METRONIC BUCHBINDER ENVOY PERCUTANEOUS CATHETERS received FDA 510(k) clearance on 1994-04-26, under 510(k) number K935425.
Who is the listed applicant for METRONIC BUCHBINDER ENVOY PERCUTANEOUS CATHETERS?
The FDA 510(k) record lists Medtronics Interventional Vascular as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for METRONIC BUCHBINDER ENVOY PERCUTANEOUS CATHETERS?
The FDA product code for METRONIC BUCHBINDER ENVOY PERCUTANEOUS CATHETERS is DQY.
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 Medtronics Interventional Vascular 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: DQY)
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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