POLYCHLOROPRENE POWDER FREE SURGICAL GLOVE (GREEN)
K-Number: K170152 · 2017-05-05
Device Summary
Frequently Asked Questions
What is the POLYCHLOROPRENE POWDER FREE SURGICAL GLOVE (GREEN)?
POLYCHLOROPRENE POWDER FREE SURGICAL GLOVE (GREEN) is a medical device that received FDA 510(k) clearance on 2017-05-05. The listed applicant is Hartalega Sdn Bhd. The 510(k) number is K170152.
When did POLYCHLOROPRENE POWDER FREE SURGICAL GLOVE (GREEN) receive FDA 510(k) clearance?
POLYCHLOROPRENE POWDER FREE SURGICAL GLOVE (GREEN) received FDA 510(k) clearance on 2017-05-05, under 510(k) number K170152.
Who is the listed applicant for POLYCHLOROPRENE POWDER FREE SURGICAL GLOVE (GREEN)?
The FDA 510(k) record lists Hartalega Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POLYCHLOROPRENE POWDER FREE SURGICAL GLOVE (GREEN)?
The FDA product code for POLYCHLOROPRENE POWDER FREE SURGICAL GLOVE (GREEN) is KGO.
Other records listing Hartalega Sdn Bhd 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: KGO)
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.