ROYAL SHIELD LATEX EXAMINATION GLOVES(TM)
K-Number: K890907 · 1989-04-26
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Device Summary
Frequently Asked Questions
What is the ROYAL SHIELD LATEX EXAMINATION GLOVES(TM)?
ROYAL SHIELD LATEX EXAMINATION GLOVES(TM) is a medical device that received FDA 510(k) clearance on 1989-04-26. The listed applicant is Shield Gloves Manufacturer Sdn. Bhd. C/O Lenty, Inc.. The 510(k) number is K890907.
When did ROYAL SHIELD LATEX EXAMINATION GLOVES(TM) receive FDA 510(k) clearance?
ROYAL SHIELD LATEX EXAMINATION GLOVES(TM) received FDA 510(k) clearance on 1989-04-26, under 510(k) number K890907.
Who is the listed applicant for ROYAL SHIELD LATEX EXAMINATION GLOVES(TM)?
The FDA 510(k) record lists Shield Gloves Manufacturer Sdn. Bhd. C/O Lenty, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ROYAL SHIELD LATEX EXAMINATION GLOVES(TM)?
The FDA product code for ROYAL SHIELD LATEX EXAMINATION GLOVES(TM) 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 Sdn. Bhd. C/O Lenty, Inc. 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
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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