PROSHIELD PLUS MULTIPLE GLOVES
K-Number: K943735 · 1994-09-16
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Device Summary
Frequently Asked Questions
What is the PROSHIELD PLUS MULTIPLE GLOVES?
PROSHIELD PLUS MULTIPLE GLOVES is a medical device that received FDA 510(k) clearance on 1994-09-16. The listed applicant is Sino (U.S.A.) Co.. The 510(k) number is K943735.
When did PROSHIELD PLUS MULTIPLE GLOVES receive FDA 510(k) clearance?
PROSHIELD PLUS MULTIPLE GLOVES received FDA 510(k) clearance on 1994-09-16, under 510(k) number K943735.
Who is the listed applicant for PROSHIELD PLUS MULTIPLE GLOVES?
The FDA 510(k) record lists Sino (U.S.A.) Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROSHIELD PLUS MULTIPLE GLOVES?
The FDA product code for PROSHIELD PLUS MULTIPLE 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 Sino (U.S.A.) Co. 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
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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