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FDA 510(k)

POWDERED VINYL PATIENT EXAMINATION GLOVES, YELLOW

K-Number: K070042 · 2007-02-23

Decision Date2007-02-23
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDERED VINYL PATIENT EXAMINATION GLOVES, YELLOW is the device name listed in this FDA 510(k) record. The listed applicant is Super Safe Plastic Products Co., Ltd.. It received FDA 510(k) clearance on 2007-02-23 under 510(k) number K070042. 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 POWDERED VINYL PATIENT EXAMINATION GLOVES, YELLOW?

POWDERED VINYL PATIENT EXAMINATION GLOVES, YELLOW is a medical device that received FDA 510(k) clearance on 2007-02-23. The listed applicant is Super Safe Plastic Products Co., Ltd.. The 510(k) number is K070042.

When did POWDERED VINYL PATIENT EXAMINATION GLOVES, YELLOW receive FDA 510(k) clearance?

POWDERED VINYL PATIENT EXAMINATION GLOVES, YELLOW received FDA 510(k) clearance on 2007-02-23, under 510(k) number K070042.

Who is the listed applicant for POWDERED VINYL PATIENT EXAMINATION GLOVES, YELLOW?

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

What is the FDA product code for POWDERED VINYL PATIENT EXAMINATION GLOVES, YELLOW?

The FDA product code for POWDERED VINYL PATIENT EXAMINATION GLOVES, YELLOW 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 Super Safe 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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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