JM GLOVES STERILE VINYL EXAMINATION
K-Number: K910775 · 1991-03-07
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Device Summary
Frequently Asked Questions
What is the JM GLOVES STERILE VINYL EXAMINATION?
JM GLOVES STERILE VINYL EXAMINATION is a medical device that received FDA 510(k) clearance on 1991-03-07. The listed applicant is Jm Gloves Co., Ltd.. The 510(k) number is K910775.
When did JM GLOVES STERILE VINYL EXAMINATION receive FDA 510(k) clearance?
JM GLOVES STERILE VINYL EXAMINATION received FDA 510(k) clearance on 1991-03-07, under 510(k) number K910775.
Who is the listed applicant for JM GLOVES STERILE VINYL EXAMINATION?
The FDA 510(k) record lists Jm Gloves Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JM GLOVES STERILE VINYL EXAMINATION?
The FDA product code for JM GLOVES STERILE VINYL EXAMINATION is LYZ.
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 Jm Gloves 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: LYZ)
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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