SHIELDTEX STERILE PATIENT EXAMINATION GLOVES
K-Number: K940387 · 1994-03-11
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Device Summary
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
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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