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FDA 510(k)

ROYAL SHIELD NON-STERILE LATEX EXAM GLOVES-BUBBLE GUM

K-Number: K943043 · 1994-09-26

Decision Date1994-09-26
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ROYAL SHIELD NON-STERILE LATEX EXAM GLOVES-BUBBLE GUM is the device name listed in this FDA 510(k) record. The listed applicant is Shield Gloves Manufacturer (M) Sdn Bhd. It received FDA 510(k) clearance on 1994-09-26 under 510(k) number K943043. 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 ROYAL SHIELD NON-STERILE LATEX EXAM GLOVES-BUBBLE GUM?

ROYAL SHIELD NON-STERILE LATEX EXAM GLOVES-BUBBLE GUM is a medical device that received FDA 510(k) clearance on 1994-09-26. The listed applicant is Shield Gloves Manufacturer (M) Sdn Bhd. The 510(k) number is K943043.

When did ROYAL SHIELD NON-STERILE LATEX EXAM GLOVES-BUBBLE GUM receive FDA 510(k) clearance?

ROYAL SHIELD NON-STERILE LATEX EXAM GLOVES-BUBBLE GUM received FDA 510(k) clearance on 1994-09-26, under 510(k) number K943043.

Who is the listed applicant for ROYAL SHIELD NON-STERILE LATEX EXAM GLOVES-BUBBLE GUM?

The FDA 510(k) record lists Shield Gloves Manufacturer (M) Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROYAL SHIELD NON-STERILE LATEX EXAM GLOVES-BUBBLE GUM?

The FDA product code for ROYAL SHIELD NON-STERILE LATEX EXAM GLOVES-BUBBLE GUM 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 Shield Gloves Manufacturer (M) Sdn Bhd 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.

View all 18 devices →

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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