NON-STERILE PATIENT EXAMINATION GLOVES
K-Number: K892303 · 1989-04-28
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Device Summary
Frequently Asked Questions
What is the NON-STERILE PATIENT EXAMINATION GLOVES?
NON-STERILE PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-04-28. The listed applicant is Starlit Ent. Co., Ltd.. The 510(k) number is K892303.
When did NON-STERILE PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?
NON-STERILE PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1989-04-28, under 510(k) number K892303.
Who is the listed applicant for NON-STERILE PATIENT EXAMINATION GLOVES?
The FDA 510(k) record lists Starlit Ent. Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-STERILE PATIENT EXAMINATION GLOVES?
The FDA product code for NON-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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