TOP QUALITY CHLORINATED-POWDERFREE EXAMINATION GLOVES
K-Number: K000050 · 2000-07-27
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Device Summary
Frequently Asked Questions
What is the TOP QUALITY CHLORINATED-POWDERFREE EXAMINATION GLOVES?
TOP QUALITY CHLORINATED-POWDERFREE EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2000-07-27. The listed applicant is Top Quality Mfg., Inc.. The 510(k) number is K000050.
When did TOP QUALITY CHLORINATED-POWDERFREE EXAMINATION GLOVES receive FDA 510(k) clearance?
TOP QUALITY CHLORINATED-POWDERFREE EXAMINATION GLOVES received FDA 510(k) clearance on 2000-07-27, under 510(k) number K000050.
Who is the listed applicant for TOP QUALITY CHLORINATED-POWDERFREE EXAMINATION GLOVES?
The FDA 510(k) record lists Top Quality Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TOP QUALITY CHLORINATED-POWDERFREE EXAMINATION GLOVES?
The FDA product code for TOP QUALITY CHLORINATED-POWDERFREE 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 Top Quality Mfg., 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
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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