INTRODUCER SHEATHS, VESSEL DILATOR, GUIDEWIRE
K-Number: K994252 · 2000-01-04
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Device Summary
Frequently Asked Questions
What is the INTRODUCER SHEATHS, VESSEL DILATOR, GUIDEWIRE?
INTRODUCER SHEATHS, VESSEL DILATOR, GUIDEWIRE is a medical device that received FDA 510(k) clearance on 2000-01-04. The listed applicant is Boston Scientific Corp. The 510(k) number is K994252.
When did INTRODUCER SHEATHS, VESSEL DILATOR, GUIDEWIRE receive FDA 510(k) clearance?
INTRODUCER SHEATHS, VESSEL DILATOR, GUIDEWIRE received FDA 510(k) clearance on 2000-01-04, under 510(k) number K994252.
Who is the listed applicant for INTRODUCER SHEATHS, VESSEL DILATOR, GUIDEWIRE?
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 INTRODUCER SHEATHS, VESSEL DILATOR, GUIDEWIRE?
The FDA product code for INTRODUCER SHEATHS, VESSEL DILATOR, GUIDEWIRE is DYB.
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: DYB)
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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