Patient Examination Gloves
K-Number: K203593 · 2021-03-19
Device Summary
Frequently Asked Questions
What is the Patient Examination Gloves?
Patient Examination Gloves is a medical device that received FDA 510(k) clearance on 2021-03-19. The listed applicant is Guangdong Kingfa Sci. & Tech.Co., Ltd.. The 510(k) number is K203593.
When did Patient Examination Gloves receive FDA 510(k) clearance?
Patient Examination Gloves received FDA 510(k) clearance on 2021-03-19, under 510(k) number K203593.
Who is the listed applicant for Patient Examination Gloves?
The FDA 510(k) record lists Guangdong Kingfa Sci. & Tech.Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Patient Examination Gloves?
The FDA product code for Patient Examination Gloves is LZA.
Other records listing Guangdong Kingfa Sci. & Tech.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.