KAEN YIH UMBILICAL CORD CLAMP
K-Number: K033846 · 2004-03-11
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Device Summary
Frequently Asked Questions
What is the KAEN YIH UMBILICAL CORD CLAMP?
KAEN YIH UMBILICAL CORD CLAMP is a medical device that received FDA 510(k) clearance on 2004-03-11. The listed applicant is Kaen Yih Enterprise Co., Ltd.. The 510(k) number is K033846.
When did KAEN YIH UMBILICAL CORD CLAMP receive FDA 510(k) clearance?
KAEN YIH UMBILICAL CORD CLAMP received FDA 510(k) clearance on 2004-03-11, under 510(k) number K033846.
Who is the listed applicant for KAEN YIH UMBILICAL CORD CLAMP?
The FDA 510(k) record lists Kaen Yih Enterprise Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KAEN YIH UMBILICAL CORD CLAMP?
The FDA product code for KAEN YIH UMBILICAL CORD CLAMP is HFW.
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: HFW)
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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