AMPRO SURGEON'S GLOVES
K-Number: K910711 · 1991-03-29
Advertisement
Device Summary
Frequently Asked Questions
What is the AMPRO SURGEON'S GLOVES?
AMPRO SURGEON'S GLOVES is a medical device that received FDA 510(k) clearance on 1991-03-29. The listed applicant is American Pro Latex, Inc.. The 510(k) number is K910711.
When did AMPRO SURGEON'S GLOVES receive FDA 510(k) clearance?
AMPRO SURGEON'S GLOVES received FDA 510(k) clearance on 1991-03-29, under 510(k) number K910711.
Who is the listed applicant for AMPRO SURGEON'S GLOVES?
The FDA 510(k) record lists American Pro Latex, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AMPRO SURGEON'S GLOVES?
The FDA product code for AMPRO SURGEON'S 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 American Pro Latex, 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.
Advertisement