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FDA 510(k)

PM GLOVE

K-Number: K905055 · 1991-01-18

Decision Date1991-01-18
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PM GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Pm Gloves, Inc.. It received FDA 510(k) clearance on 1991-01-18 under 510(k) number K905055. 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 PM GLOVE?

PM GLOVE is a medical device that received FDA 510(k) clearance on 1991-01-18. The listed applicant is Pm Gloves, Inc.. The 510(k) number is K905055.

When did PM GLOVE receive FDA 510(k) clearance?

PM GLOVE received FDA 510(k) clearance on 1991-01-18, under 510(k) number K905055.

Who is the listed applicant for PM GLOVE?

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

What is the FDA product code for PM GLOVE?

The FDA product code for PM 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 Pm Gloves, Inc. 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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