SYNTHETIC, POWDER-FREE NITRILE EXAMINATION
K-Number: K102593 · 2010-12-20
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Device Summary
Frequently Asked Questions
What is the SYNTHETIC, POWDER-FREE NITRILE EXAMINATION?
SYNTHETIC, POWDER-FREE NITRILE EXAMINATION is a medical device that received FDA 510(k) clearance on 2010-12-20. The listed applicant is Zibo Yinghao Medical Products Co., Ltd.. The 510(k) number is K102593.
When did SYNTHETIC, POWDER-FREE NITRILE EXAMINATION receive FDA 510(k) clearance?
SYNTHETIC, POWDER-FREE NITRILE EXAMINATION received FDA 510(k) clearance on 2010-12-20, under 510(k) number K102593.
Who is the listed applicant for SYNTHETIC, POWDER-FREE NITRILE EXAMINATION?
The FDA 510(k) record lists Zibo Yinghao Medical Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNTHETIC, POWDER-FREE NITRILE EXAMINATION?
The FDA product code for SYNTHETIC, POWDER-FREE NITRILE EXAMINATION is LYZ.
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 Zibo Yinghao Medical Products Co., Ltd. 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: LYZ)
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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