STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE
K-Number: K012282 · 2001-08-06
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Device Summary
Frequently Asked Questions
What is the STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE?
STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE is a medical device that received FDA 510(k) clearance on 2001-08-06. The listed applicant is Cypress Medical Products, Ltd.. The 510(k) number is K012282.
When did STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE receive FDA 510(k) clearance?
STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE received FDA 510(k) clearance on 2001-08-06, under 510(k) number K012282.
Who is the listed applicant for STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE?
The FDA 510(k) record lists Cypress Medical Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE?
The FDA product code for STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE 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 Cypress Medical Products, 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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