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FDA 510(k)

STERILE NATURAL LATEX SURGICAL GLOVES

K-Number: K892108 · 1989-09-08

Decision Date1989-09-08
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE NATURAL LATEX SURGICAL GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Ruhn Chang Industrial Co., Ltd.. It received FDA 510(k) clearance on 1989-09-08 under 510(k) number K892108. 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 STERILE NATURAL LATEX SURGICAL GLOVES?

STERILE NATURAL LATEX SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 1989-09-08. The listed applicant is Ruhn Chang Industrial Co., Ltd.. The 510(k) number is K892108.

When did STERILE NATURAL LATEX SURGICAL GLOVES receive FDA 510(k) clearance?

STERILE NATURAL LATEX SURGICAL GLOVES received FDA 510(k) clearance on 1989-09-08, under 510(k) number K892108.

Who is the listed applicant for STERILE NATURAL LATEX SURGICAL GLOVES?

The FDA 510(k) record lists Ruhn Chang Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE NATURAL LATEX SURGICAL GLOVES?

The FDA product code for STERILE NATURAL 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 Ruhn Chang Industrial Co., Ltd. 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

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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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