EUDERMIC PF POWDER-FREE SURGICAL GLOVES
K-Number: K001343 · 2000-06-12
Device Summary
Frequently Asked Questions
What is the EUDERMIC PF POWDER-FREE SURGICAL GLOVES?
EUDERMIC PF POWDER-FREE SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 2000-06-12. The listed applicant is Maxxim Medical, Inc.. The 510(k) number is K001343.
When did EUDERMIC PF POWDER-FREE SURGICAL GLOVES receive FDA 510(k) clearance?
EUDERMIC PF POWDER-FREE SURGICAL GLOVES received FDA 510(k) clearance on 2000-06-12, under 510(k) number K001343.
Who is the listed applicant for EUDERMIC PF POWDER-FREE SURGICAL GLOVES?
The FDA 510(k) record lists Maxxim Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EUDERMIC PF POWDER-FREE SURGICAL GLOVES?
The FDA product code for EUDERMIC PF POWDER-FREE SURGICAL GLOVES is KGO.
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 Maxxim Medical, Inc. 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.