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FDA 510(k)

THE ROYAL GLOVES (PATIENT EXAM GLOVES)

K-Number: K891958 · 1989-06-19

Decision Date1989-06-19
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE ROYAL GLOVES (PATIENT EXAM GLOVES) is the device name listed in this FDA 510(k) record. The listed applicant is Taizhu Latex Glove Factory , Ltd.. It received FDA 510(k) clearance on 1989-06-19 under 510(k) number K891958. 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 THE ROYAL GLOVES (PATIENT EXAM GLOVES)?

THE ROYAL GLOVES (PATIENT EXAM GLOVES) is a medical device that received FDA 510(k) clearance on 1989-06-19. The listed applicant is Taizhu Latex Glove Factory , Ltd.. The 510(k) number is K891958.

When did THE ROYAL GLOVES (PATIENT EXAM GLOVES) receive FDA 510(k) clearance?

THE ROYAL GLOVES (PATIENT EXAM GLOVES) received FDA 510(k) clearance on 1989-06-19, under 510(k) number K891958.

Who is the listed applicant for THE ROYAL GLOVES (PATIENT EXAM GLOVES)?

The FDA 510(k) record lists Taizhu Latex Glove Factory , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE ROYAL GLOVES (PATIENT EXAM GLOVES)?

The FDA product code for THE ROYAL GLOVES (PATIENT EXAM 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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