LATEX NON-STERILE EXAM GLOVES
K-Number: K890496 · 1989-04-28
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Device Summary
Frequently Asked Questions
What is the LATEX NON-STERILE EXAM GLOVES?
LATEX NON-STERILE EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1989-04-28. The listed applicant is Cal-American Exports, Inc.. The 510(k) number is K890496.
When did LATEX NON-STERILE EXAM GLOVES receive FDA 510(k) clearance?
LATEX NON-STERILE EXAM GLOVES received FDA 510(k) clearance on 1989-04-28, under 510(k) number K890496.
Who is the listed applicant for LATEX NON-STERILE EXAM GLOVES?
The FDA 510(k) record lists Cal-American Exports, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX NON-STERILE EXAM GLOVES?
The FDA product code for LATEX NON-STERILE EXAM GLOVES 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 Cal-American Exports, 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: 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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