VP SHEATH
K-Number: K051580 · 2005-10-31
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Device Summary
Frequently Asked Questions
What is the VP SHEATH?
VP SHEATH is a medical device that received FDA 510(k) clearance on 2005-10-31. The listed applicant is Flowcardia, Inc.. The 510(k) number is K051580.
When did VP SHEATH receive FDA 510(k) clearance?
VP SHEATH received FDA 510(k) clearance on 2005-10-31, under 510(k) number K051580.
Who is the listed applicant for VP SHEATH?
The FDA 510(k) record lists Flowcardia, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VP SHEATH?
The FDA product code for VP SHEATH 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 Flowcardia, 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: 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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