PROTEGRITY STEILE LATEX SURGICAL GLOVES WITH COATING
K-Number: K033905 · 2004-04-27
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Device Summary
Frequently Asked Questions
What is the PROTEGRITY STEILE LATEX SURGICAL GLOVES WITH COATING?
PROTEGRITY STEILE LATEX SURGICAL GLOVES WITH COATING is a medical device that received FDA 510(k) clearance on 2004-04-27. The listed applicant is Cardinalhealth. The 510(k) number is K033905.
When did PROTEGRITY STEILE LATEX SURGICAL GLOVES WITH COATING receive FDA 510(k) clearance?
PROTEGRITY STEILE LATEX SURGICAL GLOVES WITH COATING received FDA 510(k) clearance on 2004-04-27, under 510(k) number K033905.
Who is the listed applicant for PROTEGRITY STEILE LATEX SURGICAL GLOVES WITH COATING?
The FDA 510(k) record lists Cardinalhealth as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROTEGRITY STEILE LATEX SURGICAL GLOVES WITH COATING?
The FDA product code for PROTEGRITY STEILE LATEX SURGICAL GLOVES WITH COATING 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 Cardinalhealth 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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