Synguard Nitrile Exam Glove
K-Number: K220442 · 2022-05-12
Device Summary
Frequently Asked Questions
What is the Synguard Nitrile Exam Glove?
Synguard Nitrile Exam Glove is a medical device that received FDA 510(k) clearance on 2022-05-12. The listed applicant is Tianjin Aoshang Outdoor Equipment Co., Ltd.. The 510(k) number is K220442.
When did Synguard Nitrile Exam Glove receive FDA 510(k) clearance?
Synguard Nitrile Exam Glove received FDA 510(k) clearance on 2022-05-12, under 510(k) number K220442.
Who is the listed applicant for Synguard Nitrile Exam Glove?
The FDA 510(k) record lists Tianjin Aoshang Outdoor Equipment Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Synguard Nitrile Exam Glove?
The FDA product code for Synguard Nitrile Exam Glove is LZA.
Other records listing Tianjin Aoshang Outdoor Equipment 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: LZA)
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.