MAXXUS POWDER FREE ORTHOPAEDIC LATEX SURGICAL GLOVES
K-Number: K962986 · 1996-09-20
Advertisement
Device Summary
Frequently Asked Questions
What is the MAXXUS POWDER FREE ORTHOPAEDIC LATEX SURGICAL GLOVES?
MAXXUS POWDER FREE ORTHOPAEDIC LATEX SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 1996-09-20. The listed applicant is Johnson & Johnson Medical, Inc.. The 510(k) number is K962986.
When did MAXXUS POWDER FREE ORTHOPAEDIC LATEX SURGICAL GLOVES receive FDA 510(k) clearance?
MAXXUS POWDER FREE ORTHOPAEDIC LATEX SURGICAL GLOVES received FDA 510(k) clearance on 1996-09-20, under 510(k) number K962986.
Who is the listed applicant for MAXXUS POWDER FREE ORTHOPAEDIC LATEX SURGICAL GLOVES?
The FDA 510(k) record lists Johnson & Johnson Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAXXUS POWDER FREE ORTHOPAEDIC LATEX SURGICAL GLOVES?
The FDA product code for MAXXUS POWDER FREE ORTHOPAEDIC LATEX 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 Johnson & Johnson 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.
Advertisement