POWDER FREE PATIENT EXAMINATION GLOVE SAFE GLOVE
K-Number: K973830 · 1998-01-16
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Device Summary
Frequently Asked Questions
What is the POWDER FREE PATIENT EXAMINATION GLOVE SAFE GLOVE?
POWDER FREE PATIENT EXAMINATION GLOVE SAFE GLOVE is a medical device that received FDA 510(k) clearance on 1998-01-16. The listed applicant is Safe Glove , Ltd.. The 510(k) number is K973830.
When did POWDER FREE PATIENT EXAMINATION GLOVE SAFE GLOVE receive FDA 510(k) clearance?
POWDER FREE PATIENT EXAMINATION GLOVE SAFE GLOVE received FDA 510(k) clearance on 1998-01-16, under 510(k) number K973830.
Who is the listed applicant for POWDER FREE PATIENT EXAMINATION GLOVE SAFE GLOVE?
The FDA 510(k) record lists Safe Glove , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER FREE PATIENT EXAMINATION GLOVE SAFE GLOVE?
The FDA product code for POWDER FREE PATIENT EXAMINATION GLOVE SAFE GLOVE 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 Safe Glove , 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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