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FDA 510(k)

MEDPRIDE LATEX EXAMINATION GLOVES

K-Number: K894569 · 1989-08-24

ApplicantTranscorp
Decision Date1989-08-24
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDPRIDE LATEX EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Transcorp. It received FDA 510(k) clearance on 1989-08-24 under 510(k) number K894569. 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 MEDPRIDE LATEX EXAMINATION GLOVES?

MEDPRIDE LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-08-24. The listed applicant is Transcorp. The 510(k) number is K894569.

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

MEDPRIDE LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1989-08-24, under 510(k) number K894569.

Who is the listed applicant for MEDPRIDE LATEX EXAMINATION GLOVES?

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

What is the FDA product code for MEDPRIDE LATEX EXAMINATION GLOVES?

The FDA product code for MEDPRIDE LATEX 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.

Other records listing Transcorp 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: 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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