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FDA 510(k)

MAXXUS LP ORTHOPAEDIC LATEX SURGICAL GLOVES

K-Number: K945157 · 1995-02-13

Decision Date1995-02-13
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MAXXUS LP 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 1995-02-13 under 510(k) number K945157. 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 LP ORTHOPAEDIC LATEX SURGICAL GLOVES?

MAXXUS LP ORTHOPAEDIC LATEX SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 1995-02-13. The listed applicant is Johnson & Johnson Medical, Inc.. The 510(k) number is K945157.

When did MAXXUS LP ORTHOPAEDIC LATEX SURGICAL GLOVES receive FDA 510(k) clearance?

MAXXUS LP ORTHOPAEDIC LATEX SURGICAL GLOVES received FDA 510(k) clearance on 1995-02-13, under 510(k) number K945157.

Who is the listed applicant for MAXXUS LP 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 LP ORTHOPAEDIC LATEX SURGICAL GLOVES?

The FDA product code for MAXXUS LP 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.

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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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