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FDA 510(k)

DIVERSI-MED STERILE LATEX SURGEON'S GLOVES

K-Number: K890289 · 1989-05-05

Decision Date1989-05-05
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DIVERSI-MED STERILE LATEX SURGEON'S GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Diversi Group, Inc.. It received FDA 510(k) clearance on 1989-05-05 under 510(k) number K890289. 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 DIVERSI-MED STERILE LATEX SURGEON'S GLOVES?

DIVERSI-MED STERILE LATEX SURGEON'S GLOVES is a medical device that received FDA 510(k) clearance on 1989-05-05. The listed applicant is Diversi Group, Inc.. The 510(k) number is K890289.

When did DIVERSI-MED STERILE LATEX SURGEON'S GLOVES receive FDA 510(k) clearance?

DIVERSI-MED STERILE LATEX SURGEON'S GLOVES received FDA 510(k) clearance on 1989-05-05, under 510(k) number K890289.

Who is the listed applicant for DIVERSI-MED STERILE LATEX SURGEON'S GLOVES?

The FDA 510(k) record lists Diversi Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIVERSI-MED STERILE LATEX SURGEON'S GLOVES?

The FDA product code for DIVERSI-MED STERILE LATEX 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.

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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