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FDA 510(k)

SHIELDTEX STERILE PATIENT EXAMINATION GLOVES

K-Number: K940387 · 1994-03-11

Decision Date1994-03-11
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHIELDTEX STERILE PATIENT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Shieldtex Sdn Bhd. It received FDA 510(k) clearance on 1994-03-11 under 510(k) number K940387. 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 SHIELDTEX STERILE PATIENT EXAMINATION GLOVES?

SHIELDTEX STERILE PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1994-03-11. The listed applicant is Shieldtex Sdn Bhd. The 510(k) number is K940387.

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

SHIELDTEX STERILE PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1994-03-11, under 510(k) number K940387.

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

The FDA 510(k) record lists Shieldtex Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHIELDTEX STERILE PATIENT EXAMINATION GLOVES?

The FDA product code for SHIELDTEX 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.

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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