POWDERED VINYL PATIENT EXAMINATION GLOVES
K-Number: K102151 · 2011-04-27
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Device Summary
Frequently Asked Questions
What is the POWDERED VINYL PATIENT EXAMINATION GLOVES?
POWDERED VINYL PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2011-04-27. The listed applicant is Hebei Tengda Plastic Co., Ltd.. The 510(k) number is K102151.
When did POWDERED VINYL PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?
POWDERED VINYL PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 2011-04-27, under 510(k) number K102151.
Who is the listed applicant for POWDERED VINYL PATIENT EXAMINATION GLOVES?
The FDA 510(k) record lists Hebei Tengda Plastic Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDERED VINYL PATIENT EXAMINATION GLOVES?
The FDA product code for POWDERED VINYL PATIENT EXAMINATION GLOVES 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 Hebei Tengda Plastic 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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