HYPO-ALLERGENIC PATIENT EXAMINATION GLOVES
K-Number: K930139 · 1993-08-24
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Device Summary
Frequently Asked Questions
What is the HYPO-ALLERGENIC PATIENT EXAMINATION GLOVES?
HYPO-ALLERGENIC PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1993-08-24. The listed applicant is Shun Thai Rubber Gloves Industry Co., Ltd.. The 510(k) number is K930139.
When did HYPO-ALLERGENIC PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?
HYPO-ALLERGENIC PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1993-08-24, under 510(k) number K930139.
Who is the listed applicant for HYPO-ALLERGENIC PATIENT EXAMINATION GLOVES?
The FDA 510(k) record lists Shun Thai Rubber Gloves Industry Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HYPO-ALLERGENIC PATIENT EXAMINATION GLOVES?
The FDA product code for HYPO-ALLERGENIC 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 Shun Thai Rubber Gloves Industry Co., Ltd. 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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