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FDA 510(k)

DERMAL GLOVES

K-Number: K932953 · 1994-06-24

ApplicantGeorge Glove Company, Inc.
Decision Date1994-06-24
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DERMAL GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is George Glove Company, Inc.. It received FDA 510(k) clearance on 1994-06-24 under 510(k) number K932953. The device is classified under product code LYU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMAL GLOVES?

DERMAL GLOVES is a medical device that received FDA 510(k) clearance on 1994-06-24. The listed applicant is George Glove Company, Inc.. The 510(k) number is K932953.

When did DERMAL GLOVES receive FDA 510(k) clearance?

DERMAL GLOVES received FDA 510(k) clearance on 1994-06-24, under 510(k) number K932953.

Who is the listed applicant for DERMAL GLOVES?

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

What is the FDA product code for DERMAL GLOVES?

The FDA product code for DERMAL GLOVES is LYU.

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Related Devices (Code: LYU)

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.

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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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