BIOSENSE WEBSTER PATIENT CABLE AND LEADWIRES
K-Number: K001390 · 2000-07-21
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Device Summary
Frequently Asked Questions
What is the BIOSENSE WEBSTER PATIENT CABLE AND LEADWIRES?
BIOSENSE WEBSTER PATIENT CABLE AND LEADWIRES is a medical device that received FDA 510(k) clearance on 2000-07-21. The listed applicant is Biosense Webster, Inc.. The 510(k) number is K001390.
When did BIOSENSE WEBSTER PATIENT CABLE AND LEADWIRES receive FDA 510(k) clearance?
BIOSENSE WEBSTER PATIENT CABLE AND LEADWIRES received FDA 510(k) clearance on 2000-07-21, under 510(k) number K001390.
Who is the listed applicant for BIOSENSE WEBSTER PATIENT CABLE AND LEADWIRES?
The FDA 510(k) record lists Biosense Webster, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOSENSE WEBSTER PATIENT CABLE AND LEADWIRES?
The FDA product code for BIOSENSE WEBSTER PATIENT CABLE AND LEADWIRES is DSA.
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 Biosense Webster, 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: DSA)
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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