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FDA 510(k)

STERILE PATIENT EXAMINATION GLOVES

K-Number: K891329 · 1989-04-04

Decision Date1989-04-04
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILE PATIENT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Galaxy Intl., Inc.. It received FDA 510(k) clearance on 1989-04-04 under 510(k) number K891329. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE PATIENT EXAMINATION GLOVES?

STERILE PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-04-04. The listed applicant is Galaxy Intl., Inc.. The 510(k) number is K891329.

When did STERILE PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?

STERILE PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1989-04-04, under 510(k) number K891329.

Who is the listed applicant for STERILE PATIENT EXAMINATION 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 STERILE PATIENT EXAMINATION GLOVES?

The FDA product code for STERILE PATIENT EXAMINATION GLOVES is LYY.

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: LYY)

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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