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FDA 510(k)

POWDER FREE VINYL PATIENT EXAMINATION GLOVE

K-Number: K070187 · 2007-02-13

Decision Date2007-02-13
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDER FREE VINYL PATIENT EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Hong DI Plastic Products Co., Ltd.. It received FDA 510(k) clearance on 2007-02-13 under 510(k) number K070187. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWDER FREE VINYL PATIENT EXAMINATION GLOVE?

POWDER FREE VINYL PATIENT EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 2007-02-13. The listed applicant is Hong DI Plastic Products Co., Ltd.. The 510(k) number is K070187.

When did POWDER FREE VINYL PATIENT EXAMINATION GLOVE receive FDA 510(k) clearance?

POWDER FREE VINYL PATIENT EXAMINATION GLOVE received FDA 510(k) clearance on 2007-02-13, under 510(k) number K070187.

Who is the listed applicant for POWDER FREE VINYL PATIENT EXAMINATION GLOVE?

The FDA 510(k) record lists Hong DI Plastic Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWDER FREE VINYL PATIENT EXAMINATION GLOVE?

The FDA product code for POWDER FREE VINYL PATIENT EXAMINATION GLOVE 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 Hong DI Plastic 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

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