NEICH NM ADVANCE CATHETER SHEATH INTRODUCER
K-Number: K020964 · 2002-10-11
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Device Summary
Frequently Asked Questions
What is the NEICH NM ADVANCE CATHETER SHEATH INTRODUCER?
NEICH NM ADVANCE CATHETER SHEATH INTRODUCER is a medical device that received FDA 510(k) clearance on 2002-10-11. The listed applicant is Neich Medical(Shenzhen)Company, Ltd.. The 510(k) number is K020964.
When did NEICH NM ADVANCE CATHETER SHEATH INTRODUCER receive FDA 510(k) clearance?
NEICH NM ADVANCE CATHETER SHEATH INTRODUCER received FDA 510(k) clearance on 2002-10-11, under 510(k) number K020964.
Who is the listed applicant for NEICH NM ADVANCE CATHETER SHEATH INTRODUCER?
The FDA 510(k) record lists Neich Medical(Shenzhen)Company, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEICH NM ADVANCE CATHETER SHEATH INTRODUCER?
The FDA product code for NEICH NM ADVANCE CATHETER SHEATH INTRODUCER 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.
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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