VINYL EXAMINATION GLOVES(MFG:KAO YING INDUSTRIAL)
K-Number: K904642 · 1990-10-19
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Device Summary
Frequently Asked Questions
What is the VINYL EXAMINATION GLOVES(MFG:KAO YING INDUSTRIAL)?
VINYL EXAMINATION GLOVES(MFG:KAO YING INDUSTRIAL) is a medical device that received FDA 510(k) clearance on 1990-10-19. The listed applicant is Predex Co. , Ltd.. The 510(k) number is K904642.
When did VINYL EXAMINATION GLOVES(MFG:KAO YING INDUSTRIAL) receive FDA 510(k) clearance?
VINYL EXAMINATION GLOVES(MFG:KAO YING INDUSTRIAL) received FDA 510(k) clearance on 1990-10-19, under 510(k) number K904642.
Who is the listed applicant for VINYL EXAMINATION GLOVES(MFG:KAO YING INDUSTRIAL)?
The FDA 510(k) record lists Predex Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VINYL EXAMINATION GLOVES(MFG:KAO YING INDUSTRIAL)?
The FDA product code for VINYL EXAMINATION GLOVES(MFG:KAO YING INDUSTRIAL) is LYZ.
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 Predex Co. , Ltd. 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: LYZ)
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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