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FDA 510(k)

MAXXUS POWDER FREE ORTHOPAEDIC LATEX SURGICAL GLOVES

K-Number: K962986 · 1996-09-20

Decision Date1996-09-20
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MAXXUS POWDER FREE ORTHOPAEDIC LATEX SURGICAL GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Medical, Inc.. It received FDA 510(k) clearance on 1996-09-20 under 510(k) number K962986. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 53 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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