POWDER-FREE LATEX EXAM GLOVE W/HYPOALLERGENIC CLAIM
K-Number: K960841 · 1996-08-15
Advertisement
Device Summary
Frequently Asked Questions
What is the POWDER-FREE LATEX EXAM GLOVE W/HYPOALLERGENIC CLAIM?
POWDER-FREE LATEX EXAM GLOVE W/HYPOALLERGENIC CLAIM is a medical device that received FDA 510(k) clearance on 1996-08-15. The listed applicant is Boston Medical Corp.. The 510(k) number is K960841.
When did POWDER-FREE LATEX EXAM GLOVE W/HYPOALLERGENIC CLAIM receive FDA 510(k) clearance?
POWDER-FREE LATEX EXAM GLOVE W/HYPOALLERGENIC CLAIM received FDA 510(k) clearance on 1996-08-15, under 510(k) number K960841.
Who is the listed applicant for POWDER-FREE LATEX EXAM GLOVE W/HYPOALLERGENIC CLAIM?
The FDA 510(k) record lists Boston Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER-FREE LATEX EXAM GLOVE W/HYPOALLERGENIC CLAIM?
The FDA product code for POWDER-FREE LATEX EXAM GLOVE W/HYPOALLERGENIC CLAIM is LYY.
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 Boston Medical 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: LYY)
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