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FDA 510(k)

MODIFIED LABELING OF SURGICAL GLOVES

K-Number: K894034 · 1989-07-14

Decision Date1989-07-14
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODIFIED LABELING OF SURGICAL GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is James River Corp.. It received FDA 510(k) clearance on 1989-07-14 under 510(k) number K894034. 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 MODIFIED LABELING OF SURGICAL GLOVES?

MODIFIED LABELING OF SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is James River Corp.. The 510(k) number is K894034.

When did MODIFIED LABELING OF SURGICAL GLOVES receive FDA 510(k) clearance?

MODIFIED LABELING OF SURGICAL GLOVES received FDA 510(k) clearance on 1989-07-14, under 510(k) number K894034.

Who is the listed applicant for MODIFIED LABELING OF SURGICAL GLOVES?

The FDA 510(k) record lists James River Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED LABELING OF SURGICAL GLOVES?

The FDA product code for MODIFIED LABELING OF 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 James River Corp. 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 15 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

View on FDA Database →

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

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