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FDA 510(k)

MORE CHAIN POWDER FREE VINYL EXAMINATION GLOVES

K-Number: K951007 · 1995-07-26

Decision Date1995-07-26
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MORE CHAIN POWDER FREE VINYL EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Allerderm Laboratories, Inc.. It received FDA 510(k) clearance on 1995-07-26 under 510(k) number K951007. 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 MORE CHAIN POWDER FREE VINYL EXAMINATION GLOVES?

MORE CHAIN POWDER FREE VINYL EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1995-07-26. The listed applicant is Allerderm Laboratories, Inc.. The 510(k) number is K951007.

When did MORE CHAIN POWDER FREE VINYL EXAMINATION GLOVES receive FDA 510(k) clearance?

MORE CHAIN POWDER FREE VINYL EXAMINATION GLOVES received FDA 510(k) clearance on 1995-07-26, under 510(k) number K951007.

Who is the listed applicant for MORE CHAIN POWDER FREE VINYL EXAMINATION GLOVES?

The FDA 510(k) record lists Allerderm Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MORE CHAIN POWDER FREE VINYL EXAMINATION GLOVES?

The FDA product code for MORE CHAIN POWDER FREE VINYL EXAMINATION GLOVES 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.

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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