SHEATH ADAPTER, MODEL SA-09847
K-Number: K021723 · 2002-08-08
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Device Summary
Frequently Asked Questions
What is the SHEATH ADAPTER, MODEL SA-09847?
SHEATH ADAPTER, MODEL SA-09847 is a medical device that received FDA 510(k) clearance on 2002-08-08. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K021723.
When did SHEATH ADAPTER, MODEL SA-09847 receive FDA 510(k) clearance?
SHEATH ADAPTER, MODEL SA-09847 received FDA 510(k) clearance on 2002-08-08, under 510(k) number K021723.
Who is the listed applicant for SHEATH ADAPTER, MODEL SA-09847?
The FDA 510(k) record lists Arrow Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SHEATH ADAPTER, MODEL SA-09847?
The FDA product code for SHEATH ADAPTER, MODEL SA-09847 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 Arrow Intl., 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: 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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