POWDERED SYNTHETIC VINYL PATIENT EXAM GLOVE
K-Number: K010663 · 2001-03-30
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Device Summary
Frequently Asked Questions
What is the POWDERED SYNTHETIC VINYL PATIENT EXAM GLOVE?
POWDERED SYNTHETIC VINYL PATIENT EXAM GLOVE is a medical device that received FDA 510(k) clearance on 2001-03-30. The listed applicant is Tong Ruhn Medical Products Co., Ltd.. The 510(k) number is K010663.
When did POWDERED SYNTHETIC VINYL PATIENT EXAM GLOVE receive FDA 510(k) clearance?
POWDERED SYNTHETIC VINYL PATIENT EXAM GLOVE received FDA 510(k) clearance on 2001-03-30, under 510(k) number K010663.
Who is the listed applicant for POWDERED SYNTHETIC VINYL PATIENT EXAM GLOVE?
The FDA 510(k) record lists Tong Ruhn Medical Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDERED SYNTHETIC VINYL PATIENT EXAM GLOVE?
The FDA product code for POWDERED SYNTHETIC VINYL PATIENT EXAM GLOVE 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 Tong Ruhn Medical Products 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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