GRAND GUARD SURGICAL GLOVES
K-Number: K892061 · 1989-05-23
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Device Summary
Frequently Asked Questions
What is the GRAND GUARD SURGICAL GLOVES?
GRAND GUARD SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 1989-05-23. The listed applicant is Galaxy Intl., Inc.. The 510(k) number is K892061.
When did GRAND GUARD SURGICAL GLOVES receive FDA 510(k) clearance?
GRAND GUARD SURGICAL GLOVES received FDA 510(k) clearance on 1989-05-23, under 510(k) number K892061.
Who is the listed applicant for GRAND GUARD SURGICAL GLOVES?
The FDA 510(k) record lists Galaxy Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GRAND GUARD SURGICAL GLOVES?
The FDA product code for GRAND GUARD 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 Galaxy Intl., 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.
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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