MICROVASIVE INSURG CHLOANGIOGRAPHIC CATHETER
K-Number: K932228 · 1993-08-10
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Device Summary
Frequently Asked Questions
What is the MICROVASIVE INSURG CHLOANGIOGRAPHIC CATHETER?
MICROVASIVE INSURG CHLOANGIOGRAPHIC CATHETER is a medical device that received FDA 510(k) clearance on 1993-08-10. The listed applicant is Boston Scientific Corp. The 510(k) number is K932228.
When did MICROVASIVE INSURG CHLOANGIOGRAPHIC CATHETER receive FDA 510(k) clearance?
MICROVASIVE INSURG CHLOANGIOGRAPHIC CATHETER received FDA 510(k) clearance on 1993-08-10, under 510(k) number K932228.
Who is the listed applicant for MICROVASIVE INSURG CHLOANGIOGRAPHIC CATHETER?
The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROVASIVE INSURG CHLOANGIOGRAPHIC CATHETER?
The FDA product code for MICROVASIVE INSURG CHLOANGIOGRAPHIC CATHETER is GBZ.
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 Boston Scientific Corp 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: GBZ)
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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