LIGHTLY POWDERED VINYL SYNTHETIC EXAMINATION GLOVES
K-Number: K972104 · 1997-08-15
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Device Summary
Frequently Asked Questions
What is the LIGHTLY POWDERED VINYL SYNTHETIC EXAMINATION GLOVES?
LIGHTLY POWDERED VINYL SYNTHETIC EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1997-08-15. The listed applicant is Shinemound Enterprise, Inc.. The 510(k) number is K972104.
When did LIGHTLY POWDERED VINYL SYNTHETIC EXAMINATION GLOVES receive FDA 510(k) clearance?
LIGHTLY POWDERED VINYL SYNTHETIC EXAMINATION GLOVES received FDA 510(k) clearance on 1997-08-15, under 510(k) number K972104.
Who is the listed applicant for LIGHTLY POWDERED VINYL SYNTHETIC EXAMINATION GLOVES?
The FDA 510(k) record lists Shinemound Enterprise, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIGHTLY POWDERED VINYL SYNTHETIC EXAMINATION GLOVES?
The FDA product code for LIGHTLY POWDERED VINYL SYNTHETIC EXAMINATION GLOVES 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 Shinemound Enterprise, Inc. 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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