SIME SURGICAL LATEX GLOVE
K-Number: K940797 · 1994-05-09
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Device Summary
Frequently Asked Questions
What is the SIME SURGICAL LATEX GLOVE?
SIME SURGICAL LATEX GLOVE is a medical device that received FDA 510(k) clearance on 1994-05-09. The listed applicant is Sime Health, Ltd.. The 510(k) number is K940797.
When did SIME SURGICAL LATEX GLOVE receive FDA 510(k) clearance?
SIME SURGICAL LATEX GLOVE received FDA 510(k) clearance on 1994-05-09, under 510(k) number K940797.
Who is the listed applicant for SIME SURGICAL LATEX GLOVE?
The FDA 510(k) record lists Sime Health, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SIME SURGICAL LATEX GLOVE?
The FDA product code for SIME SURGICAL LATEX GLOVE is KGO.
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 Sime Health, 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: KGO)
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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