PATIENT EXAMINATION GLOVES, LATEX
K-Number: K894454 · 1989-09-26
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Device Summary
Frequently Asked Questions
What is the PATIENT EXAMINATION GLOVES, LATEX?
PATIENT EXAMINATION GLOVES, LATEX is a medical device that received FDA 510(k) clearance on 1989-09-26. The listed applicant is Windwell Agencies Sdn. Bhd.. The 510(k) number is K894454.
When did PATIENT EXAMINATION GLOVES, LATEX receive FDA 510(k) clearance?
PATIENT EXAMINATION GLOVES, LATEX received FDA 510(k) clearance on 1989-09-26, under 510(k) number K894454.
Who is the listed applicant for PATIENT EXAMINATION GLOVES, LATEX?
The FDA 510(k) record lists Windwell Agencies Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT EXAMINATION GLOVES, LATEX?
The FDA product code for PATIENT EXAMINATION GLOVES, LATEX 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 Windwell Agencies 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.
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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