NITRILE RUBBER POWDER-FREE EXAMINATION GLOVE
K-Number: K932404 · 1994-05-18
Advertisement
Device Summary
Frequently Asked Questions
What is the NITRILE RUBBER POWDER-FREE EXAMINATION GLOVE?
NITRILE RUBBER POWDER-FREE EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1994-05-18. The listed applicant is Safeskin Corp.. The 510(k) number is K932404.
When did NITRILE RUBBER POWDER-FREE EXAMINATION GLOVE receive FDA 510(k) clearance?
NITRILE RUBBER POWDER-FREE EXAMINATION GLOVE received FDA 510(k) clearance on 1994-05-18, under 510(k) number K932404.
Who is the listed applicant for NITRILE RUBBER POWDER-FREE EXAMINATION GLOVE?
The FDA 510(k) record lists Safeskin Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NITRILE RUBBER POWDER-FREE EXAMINATION GLOVE?
The FDA product code for NITRILE RUBBER POWDER-FREE EXAMINATION GLOVE is FMC.
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 Safeskin Corp. 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: FMC)
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.
Advertisement