Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SURGICAL LATEX STERILE GLOVES

K-Number: K892056 · 1989-06-08

Decision Date1989-06-08
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL LATEX STERILE GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Modern Rubber Industrial Co., Ltd.. It received FDA 510(k) clearance on 1989-06-08 under 510(k) number K892056. 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 SURGICAL LATEX STERILE GLOVES?

SURGICAL LATEX STERILE GLOVES is a medical device that received FDA 510(k) clearance on 1989-06-08. The listed applicant is Modern Rubber Industrial Co., Ltd.. The 510(k) number is K892056.

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

SURGICAL LATEX STERILE GLOVES received FDA 510(k) clearance on 1989-06-08, under 510(k) number K892056.

Who is the listed applicant for SURGICAL LATEX STERILE GLOVES?

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

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

The FDA product code for SURGICAL LATEX STERILE 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 Modern Rubber 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

View on FDA Database →

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

↑