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FDA 510(k)

HYGIENEX EXAMINATION GLOVES

K-Number: K922903 · 1993-02-18

Decision Date1993-02-18
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HYGIENEX EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Hygienex Corp.. It received FDA 510(k) clearance on 1993-02-18 under 510(k) number K922903. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYGIENEX EXAMINATION GLOVES?

HYGIENEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1993-02-18. The listed applicant is Hygienex Corp.. The 510(k) number is K922903.

When did HYGIENEX EXAMINATION GLOVES receive FDA 510(k) clearance?

HYGIENEX EXAMINATION GLOVES received FDA 510(k) clearance on 1993-02-18, under 510(k) number K922903.

Who is the listed applicant for HYGIENEX EXAMINATION GLOVES?

The FDA 510(k) record lists Hygienex Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYGIENEX EXAMINATION GLOVES?

The FDA product code for HYGIENEX EXAMINATION GLOVES is LYY.

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: LYY)

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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